Medico Economic Evaluation of Dermal Substitute Integra® for Coverage of Inferior Limb Traumatic Skin Loss (INTEGRA®)
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|ClinicalTrials.gov Identifier: NCT00906672|
Recruitment Status : Completed
First Posted : May 21, 2009
Last Update Posted : May 8, 2014
|Condition or disease||Intervention/treatment||Phase|
|Leg Injuries Ankle Injuries Foot Injuries||Device: INTEGRA® Procedure: Flap technique||Phase 3|
Traumatic skin loss with bone or tendon exposure essentially affects inferior limbs. There are considered serious as they often lead to functional and esthetical consequences, and they generally affect young people.
Flap surgery is the treatment of reference for these skin losses. This technique requires expensive material and a lot of medical staff. The intervention and duration of hospitalisation are often long with heavy medication. Post surgery complications or disabling sequelea involve surgical re-interventions which increase duration of hospital stay and medical staff availability.
The dermal substitute Integra® (Integra LifeSciences Corporation) is an advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone layer). This medical device allows formation of a neoderm. The silicon layer is a temporary layer which is removed when the neoderm is totally built. This surgery is fast, non-invasive, with short hospital stay and limited complications which can be treated easily.
Objective of the study: to assess medico-economic interest of innovative surgery using dermal substitute Integra® compared to the reference using flap surgery in the treatment of traumatic skin loss of inferior limbs. Assessment will be based on re-interventions incidence, long-term functional and esthetical scar results and total cost of each technique.
Study design: multicenter, randomized, open label, parallel design, clinical trial in 12 French plastic surgery / burn care centres.
Planned number of enrolled patients: 120 (80 patients receiving Integra® and 40 patients receiving the flap surgery). Patients will be randomized in 1 of the 2 groups, with an imbalance in favour of the innovative technique.
Duration of enrollment: 24 months Duration of patient follow up: 18 months
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||72 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Study Start Date :||June 2009|
|Primary Completion Date :||January 2014|
|Study Completion Date :||January 2014|
A plaque of dermal substitute Integra® is adjusted to the size of the wound and sutured. A negative pressure bandage is placed on the wound. 7 to 11 days post surgery, the Integra® silicone layer is removed and the neoderm is covered with a skin graft.
|Active Comparator: Flap technique||
Procedure: Flap technique
A flap is a part of skin, cutaneous tissue or muscle that is taken from an healthy area of the body and put on the damaged area for coverage.
- Occurrence of at least one complication requiring a surgical re-intervention [ Time Frame: Within the first 18 months after surgery ]
- Persistence of an important / major trouble of the scar measured by a "scar-trouble scale" filled in by the patient. [ Time Frame: at 18 month-follow up ]
- Auto-evaluation of patient's scar esthetical result with a visual analog scale. [ Time Frame: at 18 month-follow up ]
- Occurrence of all post surgical complications [ Time Frame: Within the first 18 months after surgery ]
- Duration of hospitalization and healing [ Time Frame: Within the first 18 months after surgery ]
- Period until return to work and re-start of daily activities [ Time Frame: Within the first 18 months after surgery ]
- Ïntensity of scar pain during cares evaluated with a visual analog scale and quality of life (EuroQol) [ Time Frame: Within the first 18 months after surgery ]
- Human and medical requirements [ Time Frame: Within the first 18 months after surgery ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00906672
|Besançon, France, 25030|
|Universiy Hospital Bordeaux,|
|Clermont-Ferrand, France, 53003|
|Grenoble, France, 38043|
|Montpellier, France, 34295|
|Saint Roch Hospital|
|Nice, France, 06003|
|Pointe-à-Pitre, France, 97159|
|Study Chair:||Geneviève CHENE, MD-PHD||USMR (University Hospital, Bordeaux)|
|Study Director:||Vincent CASOLI, MD-MHD||University Hospital, Bordeaux|