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NCT Number: NCT06841419

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

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.

Recruiting

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sohag university Hospitals

Sohag, 82511, Egypt

Location status: Recruiting

Location contact

Abdelnaser Mohamed Ahmed, resident in plastic surgery

CONTACT

[email protected]

+20 1550435303

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

surgical reconstruction of a soft tissue defects by a pedicled flap

Procedure

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 outcomes

  1. Flap Survival Rate

    Time frame: "From enrollment to the end of treatment at 8 weeks"

    The 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 outcomes

  1. Range of Motion in Reconstructed Area

    Time frame: "From enrollment to the end of treatment at 8 weeks"

    Assessment of the range of motion in the reconstructed area. Unit: Degrees. Measurement Tool: Goniometer.

  2. Strength in Reconstructed Area

    Time frame: "From enrollment to the end of treatment at 8 weeks"

    Evaluation of muscle strength in the reconstructed area. Unit: Newton (N). Measurement Tool: Dynamometer.

Study contacts

Contact information is provided by the study sponsor or research team.

Abdelnaser Mohamed Ahmed, resident in Plastic surgery

CONTACT

[email protected]

+20 01550435303

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 24, 2025
Registry last updated
May 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.