Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07084740

Study and Modeling of Perforator Flap Vascularization

Led by University Hospital, Montpellier · Updated on 2026-04-13

20

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of reconstructive surgery is to restore physical integrity altered by trauma, congenital malformations or cancerous pathologies. Several techniques are available, including flap surgery, which enables tissue to be moved from one anatomical location to another. Perforating skin/subcutaneous flaps are segments of skin and subcutaneous cellular tissue vascularized by a feeder vascular pedicle. This surgical technique has virtually zero donor-site morbidity, as it is no longer necessary to harvest muscle to ensure reliable vascularization of the flap. Flap vascularization is a variable mechanism, complex to describe and understand. For cutaneous and subcutaneous (fatty) flaps, which account for the majority of flaps used, perforator flaps (vascularized by a subcutaneous perforator artery) have become the benchmark. Unfortunately, their vascularization is currently poorly understood, and depends on experimental work carried out on fresh cadaveric anatomical specimens. These cadaveric studies fail to take into account several key factors influencing perforasomes (perforasome: skin territory vascularized by a pedicle), namely body temperature, blood pressure, heart rate, intraoperative patient position and biological parameters.

CONDITIONS

Official Title

Study and Modeling of Perforator Flap Vascularization

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 70
  • Undergoing reconstructive surgery using pedicled or free perforating flap
  • Flap has a surface area of at least 50 cm2 for good perfusion visualization
  • For pedicled perforating flaps: patient has pelvic eschar
  • For free perforating flaps: patient has traumatic pathology of lower and/or upper limb
Not Eligible

You will not qualify if you...

  • No consent obtained
  • No social security affiliation
  • Persons under court protection
  • Persons participating in another study with an exclusion period still in progress

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Montpellier

Montpellier, France, 34000

Actively Recruiting

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Research Team

C

Christian HERLIN, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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