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Recruiting NCT06841419

Reliability and Versatility of Pedicled Anterolateral Thigh Flap in Reconstruction of Soft Tissue Defects

No phase Interventional Post Traumatic Soft Tissue Defects That Could be Reached by Pedicled Anterolateral Thigh Flap Post Tumor Excision Soft Tissue Defects Post Debridement Soft Tissue Defects

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: surgical reconstruction of a soft tissue defects by a pedicled flap.
Who it may be relevant to
Registry conditions: Post Traumatic Soft Tissue Defects That Could be Reached by Pedicled Anterolateral Thigh Flap, Post Tumor Excision Soft Tissue Defects, Post Debridement Soft Tissue Defects. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

a prospective case series study for evaluation of the reliability and versatility of pedicled anterolateral thigh flap in the reconstruction of soft tissue defects as regards flap survival and complications, donor site morbidity and aesthetic outcome.

Interventions

  • Procedure surgical reconstruction of a soft tissue defects by a pedicled flap
    harvesting of a fasciocutaneous flap from the anterolateral aspect of thigh based on a perforators from the descending branch of lateral femoral circumflex artery to reconstruct a neighboring soft tissue defect.

Primary outcome measures

  • Flap Survival Rate [Time frame: "From enrollment to the end of treatment at 8 weeks"]
Secondary outcome measures (2)
  • Range of Motion in Reconstructed Area [Time frame: "From enrollment to the end of treatment at 8 weeks"]
  • Strength in Reconstructed Area [Time frame: "From enrollment to the end of treatment at 8 weeks"]

Eligibility criteria

Inclusion criteria

  • All patients with clean hip, thighs or lower abdomen defects either traumatic or non\_traumatic that cannot be closed primarily.

Exclusion criteria

  • Patients with possible compromise of vascular pedicle due to previous trauma or surgery.
  • Patient refusal

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Sohag university Hospitals — Sohag

Identifiers

NCT: NCT06841419 · Soh-Med--12-1-03MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗