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NCT07354152Recruiting

COmparison of the Use of a PERforator Flap Versus Total Skin GRAft in the Management of Loss of Substance After Resection of Cutaneous Melanoma - Pilot Study

Source: ClinicalTrials.gov · Last updated 24 Jun 2026

Brief summary (registry, in English)

Melanoma is an aggressive and potentially fatal skin cancer and was the fifth most commonly diagnosed cancer among both men and women in the United States in 2022. When detected early, cutaneous melanoma has a favorable prognosis, with a 5-year survival rate exceeding 90%. Because melanoma frequently affects younger patients, wide local excision according to international guidelines may result in substantial functional and aesthetic morbidity. Reconstruction is therefore a critical component of locoregional management and should aim to optimize functional and aesthetic outcomes without compromising oncologic control. To date, no consensus exists regarding the optimal reconstructive strategy. Skin grafts are often favored for their presumed ability to facilitate early detection of local recurrence but are associated with donor-site morbidity and suboptimal morphofunctional outcomes. Flap reconstruction has been reported to improve healing time and aesthetic results; however, it is not commonly considered first-line after melanoma excision, largely due to the unsubstantiated concern that flaps may delay recurrence detection. Notably, objective data supporting this concern are lacking. Only two retrospective studies have addressed this issue. The largest, including 165 patients, reported that perforator-based pedicled flaps achieved favorable functional and aesthetic outcomes without adversely affecting locoregional disease control. A smaller study of facial melanoma similarly found immediate reconstruction with a facial artery perforator flap to be safe and aesthetically satisfactory. In our institution, both skin grafts and flap reconstructions are used following multidisciplinary discussion. We therefore aim to comparatively evaluate wound healing after margin re-excision and patient-reported quality of life following melanoma excision, regardless of tumor stage or location, to determine whether one reconstructive approach provides superior clinical or functional benefit in routine practice.

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
6 Jan 2026
Start date
Feb 2026
Primary completion date
May 2027
Lead sponsor
Nantes University Hospital
Diseases
Melanoma
NCT number
NCT07354152

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From Feb 2026 to the primary completion date, May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Surgical contraindication to perforator flap reconstruction

Other

  • Patients with microscopic or macroscopic nodal involvement when the sentinel lymph node has been removed
  • Patients with distant metastases identified on ultrasound and/or CT scan and/or PET-CT, when performed
  • Pregnant or breastfeeding women
  • Patients without health insurance coverage
  • Vulnerable individuals: persons deprived of liberty, under legal guardianship, or under curatorship

Who the study is looking for

  • Adult men or women (≥ 18 years)
  • Patients with cutaneous melanoma of any stage (I, II, or III) according to the AJCC Cancer Staging Manual, 8th edition (2017), diagnosed prior to surgery
  • Non-closable surgical defect after margin re-excision

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Nantes-Department of Severe Burns and Aesthetic Surgery
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NantesFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.