Perforator Mapping and Optimizing Design of the Lateral Arm Flap

Aswan University

Status: Enrolling

Conditions: Coverage of Soft Tissue Defects

Treatments: Procedure: supra facial dissection; Diagnostic Test: coloured duplex

Study type: Interventional

Funder types: Other

Identifiers

NCT05718635

AswanU

Details and patient eligibility

About

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.

Enrollment: 30 estimated patients

Sex: All

Ages: 16+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• adult patients

Exclusion criteria

• children injury to pedicle

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

patients candidate for lateral arm flap

Experimental group

Treatment:

Procedure: supra facial dissection

Diagnostic Test: coloured duplex