Perforator Mapping and Optimizing Design of the Lateral Arm Flap

Not Applicable

Recruiting

• Conditions: Coverage of Soft Tissue Defects

• Registration Number: NCT05718635
• Lead Sponsor: Aswan University

Brief Summary

The goal of this clinical trial is to optimize the design of lateral arm flap. Colored duplex will be done for all Participants and compared to intra operative findings.

flap modification (Supra facial) dissection to lateral arm flap will be done and the results will compared to the ordinary method of dissection.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-10-01
• Study First Submitted: 2022-10-12
• Study First Submitted QC: 2023-01-30
• Study First Posted: 2023-02-08
• Status Verified: 2023-03
• Primary Completion: 2023-03-26
• Last Update Submitted: 2023-03-26
• Last Update Posted: 2023-03-28
• Study Completion: 2023-06-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• adult patients

Exclusion Criteria

• children injury to pedicle

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
numbers of perforators	two years	numbers of perforators in the flap
Size of perforators	two years	size in millimeter
site of perforators	two years	distance from lateral humeral epicondyle in CM

Trial Locations

Locations (1)

Faculty of Medicine; 🇪🇬 Aswan, Egypt