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UrgoStart Plus Pad

Leg ulcers, diabetic foot ulcers and pressure ulcers take an average of 210 days to heal.(1)

UrgoStart Plus Pad is a local treatment that is effective at every wound phase to reduce healing time by an average of 100 days.(4)

PROPERTIES

UrgoStart Plus Pad is effective at every wound healing phase, from the start* and through to complete healing.

This dressing:

  • Desloughs and absorbs exudates thanks to its polyabsorbent fibres.
  • Reduces healing time thanks to its patented TLC-NOSF** matrix.

The efficacy of TLC-NOSF on the reduction of healing time has been demonstrated in double-blind, randomised controlled clinical studies (2,3) and by an analysis of observational studies.(4) The earlier TLC-NOSF treatment is started, the more effective it is(3,4).

UrgoStart Plus Pad is highly conformable and can be cut to fit the shape and size of the wound. It is suitable for damaged surrounding skin. It can also be juxtaposed and used under compression.

Finally, UrgoStart Plus Pad is always used as part of a global management approach, along with appropriate etiological treatment.

 

INDICATIONS

UrgoStart Plus Pad is a dressing indicated for all healing phases* (from the desloughing phase* through to hea

ling) in the treatment of chronic exuding wounds (leg ulcers, pressure ulcers, diabetic foot ulcers) and acute wounds that have become chronic.

Contraindications:

  • UrgoStart Plus Pad helps control minor bleeding. However, it should not be used for heavily bleeding wounds.
  • To prevent any risk of delay in appropriate treatment, UrgoStart Plus Pad is contraindicated in cancerous wounds and in wounds demonstrating deep abscess formation.
  • Do not use UrgoStart Plus Pad in the event of known sensitivity to the dressing.
  •  

INSTRUCTION FOR USE

. Wound preparation:

  • Clean the wound using the conventional care protocol, then rinse with normal saline.
  • If an antiseptic has previously been used, rinse the wound carefully with normal saline before applying UrgoStart Plus Pad.
  • Carefully dry the skin around the wound.
  • The use of UrgoStart Plus Pad does not dispense with the need for mechanical debridement when required.
  1. Dressing application:
  • Carefully remove the protective tabs.
  • Apply with the micro-adherent side of the UrgoStart Plus Pad dressing in contact with the wound. UrgoStart Plus Pad can be cut using sterile scissors to fit the dressing size to the wound if required.
  • If necessary, cover with a secondary dressing suitable for the location and exuding nature of the wound.
  • Apply a compression bandage over the dressing where prescribed.
  1. Dressing removal:
  • Pressing on healthy skin, lift a corner of the dressing and remove it carefully.
  1. Dressing changes:
  • Remove the entire dressing when it is saturated and clean the wound if required. It is recommended that the UrgoStart Plus Pad dressing be changed every 1 to 2 days during the wound desloughing phase, then as often as required by the volume of exudates and the clinical progress of the wound. It can be left in place for up to 7 days.
  • Discard any unused parts of the dressing.

Precautions for use:

  • The micro-adherent mass of the UrgoStart Plus Pad dressing sticks to latex surgical gloves. Therefore it is recommended that the tabs be used to facilitate application of the dressing.
  • If the wound shows signs of local infection, it is recommended that the bacterial component be treated first with an antimicrobial dressing (such as UrgoClean Ag) before starting treatment with UrgoStart Plus Pad.
  • In the event of an atypical ulcer demonstrating induration or excessive granulation, treatment with UrgoStart Plus Pad should only be started after having verified the absence of any ulcer deterioration, to prevent any delay in diagnosis.
  • In the absence of clinical data in the context of Epidermolysis bullosa (irrespective of its duration), the use of UrgoStart Plus Pad dressings is not recommended.
  • Stinging or even painful sensations can be reported at the start of treatment: these are generally related to the healing process and rarely warrant suspension of treatment.
  • During desloughing, the wound may appear to get larger due to gradual elimination of slough.
  • The concomitant use of a cream, lotion, ointment or emulsion is not recommended.
  • Sterile individual packaging, for single use: reuse of a disposable dressing can lead to risks of infection.
  • Do not re-sterilise the dressing.
  • Check that the sterility protector is intact before use. Do not use if the packaging is damaged.

 

FORMATS

CLINICAL EVIDENCES

In 2012, the Journal of Wound Care published the CHALLENGE(5) study, demonstrating that TLC-NOSF treatment leads to a greater reduction in wound surface area compared to a neutral dressing.

 

 

 

In December 2018, The Lancet Diabetes & Endocrinology international medical journal published the EXPLORER(2) clinical trial, demonstrating that TLC-NOSF treatment heals 60% more patients compared to a neutral dressing and that the earlier TLC-NOSF treatment is started, the more effective it is(3).

 

 

The REALITY(4) analysis, published in 2017 in the Journal of Wound Care, presents a compilation of eight observational studies conducted in more than 10,000 patients and shows that TLC-NOSF reduces the healing time of chronic wounds by an average of 100 days and that the earlier TLC-NOSF treatment is started, the more effective it is.

 

In 2020, the Journal of Wound Care published the last URGOSTART PLUS OBSERVATIONAL STUDY conducted in 1,140 patients, demonstrating that UrgoStart Plus is effective irrespective of the wound type, whatever the wound phase and however long it has been present(6).

 

The HAS (French National Authority for Health) has granted the entire range a level III clinical added value (CAV)(7) something that is unprecedented for a dressing.

 

The URGO Group was awarded the 2018 Galien France medical device prize for UrgoStart®. Each year, this prestigious award recognises exceptional innovations in the field of health.

 

In January 2019, the United Kingdom’s NICE (National Institute for Health and Care Excellence) recommended TLC-NOSF treatment for the wound care of diabetic foot ulcers and venous leg ulcers(8). The NICE recommendations support the fact that the UrgoStart® range has better results in terms of reducing wound healing time, improving patients’ quality of life and enabling significant savings for health authorities compared to neutral dressings.

2019: IWGDF (International Working Group on the Diabetic Foot) guidelines This is the very first time that a dressing has been recommended by the IWGDF(9).

 

 
References:
*Excluding dry necrosis. **TLC-NOSF: Lipido-Colloid technology – Nano OligaSaccharide Factor (KSOS: Potassium octasulfate sucrose salt).
1. Report to the French minister responsible for Social Security and the French Parliament concerning the evolution of French National Health Insurance charges and products for 2014. July 2013. CNAM database: leg ulcers: 210 days; pressure ulcers: 223 days; diabetic foot ulcers: comparative data not available.
2. Edmonds M et al. Sucrose octasulfate dressing versus control dressing in patients with neuroischaemic diabetic foot ulcers (Explorer): an international, multicentre, double-blind, randomised, controlled trial. Lancet Diabetes Endocrinol. 2018 Mar; 6(3): 186-196.
3. Lázaro-Martínez JL et al. Optimal wound closure of diabetic foot ulcers with early initiation of TLC-NOSF treatment: post-hoc analysis of Explorer. J Wound Care. 2019 Jun 2; 28(6): 358-367.
4. Münter KC et al. The reality of routine practice: a pooled data analysis on chronic wounds treated with TLC-NOSF wound dressings. J Wound Care. 2017 Feb; 26 (Sup2): S4-S15. Erratum in: J Wound Care. 2017 Mar 2; 26(3): 153.
5. Meaume S et al. A randomized, controlled, double-blind prospective trial with a Lipido-Colloid Technology-Nano-OligoSaccharide Factor wound dressing in the local management of venous leg ulcers. Wound Repair Regen. 2012; 20(4): 500-511.
6. Dissemond J. et al. Clinical evaluation of polyabsorbent TLC-NOSF dressings on chronic wounds: a prospective, observational, multicentre study of 1140 patients. J Wound Care. 2020; 29(6): 350-361.
7. CAV III: in non-infected (IDSA/IWGDF infection criteria) neuro-ischaemic diabetic foot ulcers (non-critical ischaemia), in the granulation phase (sequential treatment).
8. In leg ulcers and diabetic foot ulcers. https://www.nice.org.uk/guidance/mtg42, January 2019.
9. In the treatment of diabetic foot ulcers. IWGDF Guidelines on the prevention and management of diabetic foot disease, 2019.
UrgoStart Plus Pad: Class IIb medical device (G-Med; 0459). Treatment to reduce healing time. LPPR fully reimbursable (Social Security: 60% + top-up mutual insurance: 40%) in the treatment of venous or mixed, predominantly venous leg ulcers in the granulation phase (sequential treatment), and in non-infected (IDSA/IWGDF infection criteria) neuro-ischaemic diabetic foot ulcers (non-critical ischaemia), in the granulation phase (sequential treatment). Read the leaflet carefully before use, particularly the precautions for use and contraindications.
Manufacturer: Laboratoires URGO – 01/2021.

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UrgoStart

UrgoStart is an absorbent hydrocellular lipido-colloid dressing with a micro-adherent TLC-NOSF matrix, an innovative technology developed by Laboratoires Urgo.

Leg ulcers, diabetic foot ulcers and pressure ulcers take an average of 210 days* to heal.(1)

*CNAM database: leg ulcers: 210 days; pressure ulcers: 223 days; diabetic foot ulcers: comparative data not available.

 

UrgoStart is a local treatment that reduces the healing time of these types of wounds by an average of 100 days.(5)

PROPERTIES

Efficacy:

  • Reduction in healing time thanks to its patented TLC-NOSF matrix.(5)

Practicality:

  • Maintenance of a moist environment that promotes healing
  • Absorption of exudates and drainage, limiting the risk of maceration.
  • UrgoStart is a conformable dressing that can be cut to fit the shape of the wound.

The efficacy of TLC-NOSF on the reduction of healing time has been demonstrated in double-blind, randomised controlled clinical studies (2,3,4) and by an analysis of observational studies.(5) The earlier TLC-NOSF treatment is started, the more effective it is.(5)

Finally, UrgoStart is always used as part of a global management approach, along with appropriate etiological treatment.

 

INDICATIONS

UrgoStart is used in patients with leg ulcers, diabetic foot ulcers and pressure ulcers, from whenever granulation tissue appears until complete healing.

Contraindications:

  • To prevent any risk of delay in appropriate treatment, UrgoStart is contraindicated in cancerous wounds and in fistular wounds demonstrating deep abscess formation.
  • Do not use UrgoStart in the event of known sensitivity to the dressing.

 

INSTRUCTIONS FOR USE

  1. Wound preparation:
  • Clean the wound using the conventional care protocol.
  • If an antiseptic has previously been used, rinse the wound carefully with normal saline before applying UrgoStart.
  • Carefully dry the skin around the wound.

UrgoStart can be cut using sterile scissors to fit the dressing size to the wound if necessary.

  1. Dressing application:

Standard form

  • Remove the protective tabs.
  • Apply the micro-adherent side of the UrgoStart dressing in contact with the wound.
  • Secure the dressing in place with a suitable bandage or tape.
  • Apply a compression bandage over the dressing where prescribed.

Heel form

  • The dressing is arrow-shaped. Remove the protective tab.
  • Position the arrow towards the front of the foot and place the heel in the centre of the micro-adherent side of the dressing.
  • Attach the back part of the arrow over the Achilles tendon.
  • Remove the side tabs and carefully apply the side parts of the dressing to either side of the foot.
  • Secure the dressing in place with a suitable bandage or tape.
  1. Dressing changes:

UrgoStart should be changed every 2 to 4 days on average, and may be left in place for up to 7 days, depending on the exudate volume and the clinical condition of the wound.
The recommended treatment duration is at least 8 weeks.

Precautions for use:

  • The micro-adherent lipido-colloid mass of UrgoStart sticks to latex surgical gloves. It is therefore recommended that the product be handled carefully, avoiding any contact with the coated surface or using sterile tongs.
  • If the wound shows signs of significant bacterial colonisation, it is recommended that the bacterial component be treated first before starting treatment with UrgoStart.
  • In the event of an atypical ulcer demonstrating induration or excessive localised granulation, treatment with UrgoStart should only be started after having verified the absence of any ulcer deterioration, to prevent any delay in diagnosis.
  • Stinging or even painful sensations have been reported, mainly at the start of treatment, with UrgoStart. These are related to the resumption of the healing process and only warrant suspension of treatment in rare cases.
  • In the absence of clinical data relative to uncomplicated acute wounds and in the context of Epidermolysis Bullosa, irrespective of duration, the use of UrgoStart is not recommended.
  • UrgoStart must not be used during hyperbaric oxygen chamber therapy without an oxygen mask (risk of combustion due to the presence of fat). This contraindication does not apply for hyperbaric oxygen chamber therapy with an oxygen mask if the oxygen concentration inside the chamber is less than 25% and if UrgoStart is not applied on the area over which the mask is placed.
  • Sterile individual packaging, for single use: reuse of a single-use dressing can lead to risks of infection.
  • Do not re-sterilise the dressing.
  • Check that the sterility protector is intact before use. Do not use if the packaging is damaged.

 

FORMATS

 

 

 

CLINICAL EVIDENCE

  1. Report to the French minister responsible for Social Security and the French Parliament concerning the evolution of French National Health Insurance charges and products for 2014. July 2013.
  2. Edmonds M, Lázaro-Martínez JL, Alfayate-García JM, Martini J, Petit JM, Rayman G, Lobmann R, Uccioli L, Sauvadet A, Bohbot S, Kerihuel JC, Piaggesi A. Sucrose octasulfate dressing versus control dressing in patients with neuroischaemic diabetic foot ulcers (Explorer): an international, multicentre, double-blind, randomised, controlled trial. Lancet Diabetes Endocrinol. 2018 Mar;6(3):186-196.
  3. Meaume S, Truchetet F, Cambazard F et al. A randomized, controlled, double-blind prospective trial with a Lipido-Colloid Technology-Nano-OligoSaccharide Factor wound dressing in the local management of venous leg ulcers. Wound Repair Regen. 2012; 20: 4, 500–511.
  4. Meaume S, Dompmartin A, Lazareth I, Sigal M, Truchetet F, Sauvadet A, Bohbot S. Quality of life in patients with leg ulcers: results from CHALLENGE, a double-blind randomized controlled trial. Journal of Wound Care. 2017; 26 (7): 368-379.
  5. Münter KC, Meaume S, Augustin M, Senet P, Kérihuel J.C. The reality of routine practice: a pooled data analysis on chronic wounds treated with TLC-NOSF wound dressings. J Wound Care. 2017 Feb; 26 (Sup2): S4-S15. Erratum in: J Wound Care. 2017 Mar 2; 26(3): 153.

 

Other products

UrgoStart Plus Pad

Details

UrgoStart Plus Border

Details

UrgoStart Contact

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UrgoClean Ag

Details

UrgoClean

UrgoClean, for complete and continuous cleansing

UrgoClean cleanses the wound of debris that impairs the healing process

 

PROPERTIES

  • Traps slough effectively (+50% lesions cleared compared to hydrofiber after 6W) and manages mild bleeding (1,2)
  • Absorbs exudate without maceration (3), protecting perilesional skin
  • Keeps the bottom of the lesion cleansed (maintenance debridement)(2,4)
  • Ensures atraumatic and painless care for the patient(2,5)

INDICATIONS

UrgoCleanis indicated for the treatment of exudative lesions in the desloughing phase (chronic lesions, acute lesions and cancerous lesions).

UrgoClean Rope is used for the treatment of cavitary lesions

 

INSTRUCTIONS FOR USE

  • Cleans the wound with physiological solution

  • Apply the micro-sticky side of the dressing in contact with the wound 
  • Use a secondary dressing depending on the volume of exudate and secure with a bandage or elastocompression therapy when prescribed

Change the dressing every 1-2 days at the beginning of the treatment and then up to 7 days, taking into account the exudate and the clinical state of the wound.

FORMATS

 

 

CLINICAL EVIDENCE

  1. Data on file Urgo, report n°88050-2009.
  2. Meaume S. et al., Evaluation of two fibrous wound dressings for the management of leg ulcers: Results of a European randomised controlled trial (EARTH RCT). J Wound Care, Vol 23, No 3; March 2014, 105-116. 
  3. Meaume S. et al., Management of chronic wounds with an innovative absorbent wound dressing. J Wound Care, Vol 21, No 7; July 2012, 315-322. 
  4. Percival SL, et al. Slough and biofilm: removal of barriers to wound healing by desloughing. J Wound Care. 2015 Nov; 24(11):498,500-3,506-10. 
  5. Meaume et al., The importance of pain reduction through dressing selection in routine wound management: the MAPP study, Journal of Wound Care, 2004, Vol 13, No 10, 409-413.

Other products

UrgoClean Ag

Details

UrgoTul Ag

Details

UrgoTul

Details

UrgoStart Plus Border

Leg ulcers, diabetic foot ulcers and pressure ulcers take an average of 210 days to heal.(1)

UrgoStart Plus Border is a local treatment that is effective at every wound phase to reduce healing time by an average of 100 days.(4)

PROPERTIES

UrgoStart Plus Border is effective at every wound healing phase*, from the start* and through to complete healing.

* excluding dry necrosis

This dressing:
– Desloughs and absorbs exudates thanks to its polyabsorbent fibres.
– Reduces healing time thanks to its healing TLC-NOSF** matrix.

The efficacy of TLC-NOSF on the reduction of healing time has been demonstrated in double-blind, randomised controlled clinical studies (2,3) and by an analysis of observational studies.(4) The earlier TLC-NOSF treatment is started, the more effective it is(3,4).

UrgoStart Plus Border is highly conformable and easy to reposition. Ready to use, it is suitable for both healthy and fragile surrounding skin.

Finally, UrgoStart Plus Border is always used as part of a global management approach, along with appropriate etiological treatment.

INDICATIONS

UrgoStart Plus Border is a dressing indicated for all healing phases* (from the desloughing phase* through to healing) in the treatment of chronic exuding wounds (leg ulcers, pressure ulcers, diabetic foot ulcers) and acute wounds that have become chronic.

*excluding dry necrosis

Contraindications:

  • UrgoStart Plus Border helps control minor bleeding. However, it should not be used for heavily bleeding wounds.
  • To prevent any risk of delay in appropriate treatment, UrgoStart Plus Border is contraindicated in cancerous wounds and in wounds demonstrating deep abscess formation.
  • Do not use UrgoStart Plus Border in the event of known sensitivity to the dressing.

INSTRUCTIONS FOR USE

1. Wound preparation:

  • Clean the wound using the conventional care protocol, then rinse with normal saline.
  • If an antiseptic has previously been used, rinse the wound carefully with normal saline before applying UrgoStart Plus Border.
  • Carefully dry the skin around the wound.
  • The use of UrgoStart Plus Border does not dispense with the need for mechanical debridement when required.

2. Dressing application:

  • Carefully remove the protective tabs.
  • Apply the micro-adherent central pad of UrgoStart Plus Border over the wound (the adhesive silicone edges must be at least 1 cm from the wound). Smooth the dressing.
  • Apply a compression bandage over the dressing where prescribed.

Application of the Sacrum format:

  • Position the dressing with the tip pointing downwards towards the bottom of the sacral region.

3. Dressing removal:

  • Pressing on healthy skin, lift a corner of the dressing and remove it carefully.

4. Dressing changes:

  • Remove the entire dressing when it is saturated and clean the wound if required. It is recommended that the UrgoStart Plus Border dressing be changed every 1 to 2 days during the wound desloughing phase, then as often as required by the volume of exudates and the clinical progress of the wound. It can be left in place for up to 7 days.
  • Discard any unused parts of the dressing.

Precautions for use:

  • The central pad, which includes a super-absorbent layer, should not be cut.
  • However, the adhesive silicone edges can be cut using sterile scissors to fit to different anatomical contours.
  • If the wound shows signs of local infection, it is recommended that the bacterial component be treated first with an antimicrobial dressing (such as UrgoClean Ag) before starting treatment with UrgoStart Plus Border.
  • In the event of an atypical ulcer demonstrating induration or excessive granulation, it is recommended that treatment with UrgoStart Plus Border only be started after having verified the absence of any ulcer deterioration, to prevent any delay in diagnosis.
  • In the context of Epidermolysis bullosa (irrespective of its duration), the use of UrgoStart Plus Border dressings is not recommended.
  • Stinging or even painful sensations can be reported at the start of treatment: these are generally related to the healing process and rarely warrant suspension of treatment.
  • During desloughing, the wound may appear to get larger due to gradual elimination of slough.
  • Shave or cut excess hair as close as possible to the skin to ensure good contact with the wound.
  • In the event of concomitant use with a cream, lotion, ointment or emulsion, allow the skin to dry before applying the dressing.
  • Sterile individual packaging, for single use: reuse of a disposable dressing can lead to risks of infection.
  • Do not re-sterilise the dressing.
  • Check that the sterility protector is intact before use. Do not use if the packaging is damaged.

FORMATS

*Dispositifs Médicaux de classe IIb (GMed 0459). Traitement pour réduire le temps de  cicatrisation. Intégralement remboursables LPPR (Sec. Soc. : 60% + Mutuelle : 40%) dans le traitement de l’ulcère de jambe veineux ou mixte à prédominance veineuse, en phase de bourgeonnement (traitement séquentiel), et dans  l’ulcère du pied chez le patient diabétique d’origine neuro-ischémique (ischémie non critique), non infecté (critères d’infection IDSA/IWGDF), en phase de bourgeonnement (traitement séquentiel).

 

CLINICAL EVIDENCE

TLC-NOSF, AN INNOVATION WITH PROVEN AND RECOGNISED EFFICACY

 

In 2012, the Journal of Wound Care published the CHALLENGE(5) study, demonstrating that TLC-NOSF treatment leads to a greater reduction in wound surface area compared to a neutral dressing.

 

 

 

In December 2018, The Lancet Diabetes & Endocrinology international medical journal published the EXPLORER(2) clinical trial, demonstrating that TLC-NOSF treatment heals 60% more patients compared to a neutral dressing and that the earlier TLC-NOSF treatment is started, the more effective it is(3).

 

 

 

The REALITY(4) analysis, published in 2017 in the Journal of Wound Care, presents a compilation of eight observational studies conducted in more than 10,000 patients and shows that TLC-NOSF reduces the healing time of chronic wounds by an average of 100 days and that the earlier TLC-NOSF treatment is started, the more effective it is.

 

 

In 2020, the Journal of Wound Care published the last URGOSTART PLUS OBSERVATIONAL STUDY conducted in 1,140 patients, demonstrating that UrgoStart Plus is effective irrespective of the wound type, whatever the wound phase and however long it has been present(6).

 

 

The HAS (French National Authority for Health) has granted the entire range a level III clinical added value (CAV)(7) something that is unprecedented for a dressing.

 

 

The URGO Group was awarded the 2018 Galien France medical device prize for UrgoStart®. Each year, this prestigious award recognises exceptional innovations in the field of health.

 

 

In January 2019, the United Kingdom’s NICE (National Institute for Health and Care Excellence) recommended TLC-NOSF treatment for the wound care of diabetic foot ulcers and venous leg ulcers(8). The NICE recommendations support the fact that the UrgoStart® range has better results in terms of reducing wound healing time, improving patients’ quality of life and enabling significant savings for health authorities compared to neutral dressings.

2019: IWGDF (International Working Group on the Diabetic Foot) guidelines This is the very first time that a dressing has been recommended by the IWGDF.(9)

 

References:
*Excluding dry necrosis. **TLC-NOSF: Lipido-Colloid technology – Nano OligaSaccharide Factor (KSOS: Potassium octasulfate sucrose salt).
1. Report to the French minister responsible for Social Security and the French Parliament concerning the evolution of French National Health Insurance charges and products for 2014. July 2013. CNAM database: leg ulcers: 210 days; pressure ulcers: 223 days; diabetic foot ulcers: comparative data not available.
2. Edmonds M et al. Sucrose octasulfate dressing versus control dressing in patients with neuroischaemic diabetic foot ulcers (Explorer): an international, multicentre, double-blind, randomised, controlled trial. Lancet Diabetes Endocrinol. 2018 Mar; 6(3): 186-196.
3. Lázaro-Martínez JL et al. Optimal wound closure of diabetic foot ulcers with early initiation of TLC-NOSF treatment: post-hoc analysis of Explorer. J Wound Care. 2019 Jun 2; 28(6): 358-367.
4. Münter KC et al. The reality of routine practice: a pooled data analysis on chronic wounds treated with TLC-NOSF wound dressings. J Wound Care. 2017 Feb; 26 (Sup2): S4-S15. Erratum in: J Wound Care. 2017 Mar 2; 26(3): 153.
5. Meaume S et al. A randomized, controlled, double-blind prospective trial with a Lipido-Colloid Technology-Nano-OligoSaccharide Factor wound dressing in the local management of venous leg ulcers. Wound Repair Regen. 2012; 20(4): 500-511.
6. Dissemond J. et al. Clinical evaluation of polyabsorbent TLC-NOSF dressings on chronic wounds: a prospective, observational, multicentre study of 1,140 patients. J Wound Care. 2020; 29(6): 350-361.
7. CAV III: in non-infected (IDSA/IWGDF infection criteria) neuro-ischaemic diabetic foot ulcers (non-critical ischaemia), in the granulation phase (sequential treatment).
8. In leg ulcers and diabetic foot ulcers. https://www.nice.org.uk/guidance/mtg42, January 2019.
9. In the treatment of diabetic foot ulcers. IWGDF Guidelines on the prevention and management of diabetic foot disease, 2019
UrgoStart Plus Pad: Class IIb medical device (G-Med; 0459). Treatment to reduce healing time. LPPR fully reimbursable (Social Security: 60% + top-up mutual insurance: 40%) in the treatment of venous or mixed, predominantly venous leg ulcers in the granulation phase (sequential treatment), and in non-infected (IDSA/IWGDF infection criteria) neuro-ischaemic diabetic foot ulcers (non-critical ischaemia), in the granulation phase (sequential treatment). Read the leaflet carefully before use, particularly the precautions for use and contraindications.
Manufacturer: Laboratoires URGO – 12/2020.

Other products

UrgoClean Ag

Details

UrgoTul

Details

UrgoK2

Details