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Perforator Mapping and Optimizing Design of the Lateral Arm Flap

NCT05718635 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2023-03-28

No results posted yet for this study

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.

Conditions

  • Coverage of Soft Tissue Defects

Interventions

DIAGNOSTIC_TEST

coloured duplex

colored duplex to locate numbers sites and size of perforators.

PROCEDURE

supra facial dissection

flap raising in supra facial plane

Sponsors & Collaborators

  • Aswan University

    lead OTHER

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-01
Primary Completion
2023-03-26
Completion
2023-06-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05718635 on ClinicalTrials.gov