The Technique of Skin Stretching for Acute Burn Treatment and Scar Reconstruction

Phase 3

Completed

• Conditions: Scars; Burns
• Interventions: Procedure: serial excision; Procedure: Split skin graft; Procedure: skin stretching device

• Registration Number: NCT00609908
• Lead Sponsor: Association of Dutch Burn Centres

Brief Summary

Objective:

A randomized controlled trial is performed to evaluate the clinical effectiveness of the skin stretching technique for two categories:

1. acute burn wounds: wound closure by means of skin stretching should lead to a significant reduction of scar surface area in comparison to the standard technique, the split skin grafting;

2. scar reconstructions: wound closure by means of skin stretching during one operative procedure should lead to a comparable scar surface in comparison to the multiple procedures techniques such as serial excision.

Study design:

Skin stretching will be compared to split skin grafting and should result in burn wound closure with significantly smaller scars. Also, a comparison will be made between the technique of serial excision versus skin stretching for scar reconstructions.

Scar evaluation three and twelve months after surgery will include the following parameters:

* surface area;

* Patient and Observer Scar Assessment Scale (POSAS);

* elasticity;

* vascularization and pigmentation;

* thickness;

* dermal architecture.

After 12 months adults will undergo a biopsy of the scar under local anesthesia. The experimental group, treated with the skin stretcher will undergo one extra biopsy of the formerly stretched skin.

Intervention:

At the start of the operation will be determined by randomization if skin stretching or split skin grafting (acute burn wounds) or serial excision (scar reconstruction category) will be performed.

Detailed Description

Eligibility criteria:

Inclusion:

1. Acute Burn wounds or scar reconstructions that require surgical treatment; 2. Sufficient healthy skin at (at least) one edge of the wound/scar must be available for the stretching procedure.

3. Age \>= 18 years

Exclusion:

1. language barrier;

2. known history of keloid formation;

3. systemic diseases: Diabetes Mellitus, immunodeficiency, arterial insufficiency;

4. local or systemic application of corticosteroids;

5. psychiatric diseases leading to study bias (e.g. automutilation);

6. skin diseases that lead to collagen and/or elastin abnormalities such as Ehlers Danlos;

7. radiated skin;

8. wound located at extremities, exceeding \>33% of circumference (acute burn category);

Primary study parameters/outcome of the study:

The primary study parameter is the surface area of the scar after 12 months

Secondary study parameters/outcome of the study (if applicable):

All scars will also be subjected to the scar evaluation protocol after 3 and 12 months by an independent observer for the evaluation of the:

* patient and observer scar assessment scale (POSAS);

* scar elasticity (Cutometer);

* scar vascularisation \& pigmentation (DermaSpectrometer);

* scar thickness (histopathology, only after 12 months).

Punch biopsies are taken for morphometry of dermal architecture (Fourier analysis). During surgery one biopsy is obtained of the normal skin. In the experimental group an additional biopsy is obtained at the end of the stretching procedure in order to be able to compare structure of the dermal matrix and orientation of the collagen fibers.

After 1 year, one biopsy is taken from the scar. The experimental group will undergo one additional biopsy of the formerly stretched skin.

Study Timeline

• Study Start: 2007-12
• Study First Submitted: 2008-01-25
• Study First Submitted QC: 2008-02-06
• Study First Posted: 2008-02-07
• Primary Completion: 2011-06
• Study Completion: 2011-06
• Status Verified: 2015-06
• Last Update Submitted: 2015-06-25
• Last Update Posted: 2015-06-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
B1	serial excision	Scar reconstruction: serial excision
A1	Split skin graft	Acute Burn Wounds: Wound debridement and split skin grafting
A2	skin stretching device	Acute Burn Wounds: excision of the burn wound and primary closure, using a skin stretching device
B2	skin stretching device	Scar reconstruction: primary closure, using skin stretching device

Primary Outcome Measures

Name	Time	Method
the surface area of the scar after 12 months	3 and 12 months after surgery

Secondary Outcome Measures

Name	Time	Method
scar evaluation protocol: - patient and observer scar assessment scale (POSAS); - scar elasticity (Cutometer); - scar vascularization & pigmentation (DermaSpectrometer); - scar thickness	3 and 12 months after surgery

Trial Locations

Locations (1)

Red Cross Hospital; 🇳🇱 Beverwijk, Netherlands