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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06841419
Enrollment
20
Registered
2025-02-24
Start date
2025-02-15
Completion date
2025-12-31
Last updated
2025-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Debridement Soft Tissue Defects, Post Traumatic Soft Tissue Defects That Could be Reached by Pedicled Anterolateral Thigh Flap, Post Tumor Excision Soft Tissue Defects

Brief summary

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

PROCEDUREsurgical 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.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Flap Survival RateFrom enrollment to the end of treatment at 8 weeksThe percentage of flaps that survive completely without necrosis or partial loss. Complications will be graded (e.g., total flap loss, partial necrosis, or marginal necrosis). Unit: Percentage. Measurement Tool: ruler/(Mesure).

Secondary

MeasureTime frameDescription
Range of Motion in Reconstructed AreaFrom enrollment to the end of treatment at 8 weeksAssessment of the range of motion in the reconstructed area. Unit: Degrees. Measurement Tool: Goniometer.
Strength in Reconstructed AreaFrom enrollment to the end of treatment at 8 weeksEvaluation of muscle strength in the reconstructed area. Unit: Newton (N). Measurement Tool: Dynamometer.

Countries

Egypt

Contacts

Primary ContactAbdelnaser Mohamed Ahmed, resident in Plastic surgery
dr.nasser5656@gmail.com+20 01550435303

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026