Perforator Mapping and Optimizing Design of the Lateral Arm Flap

Perforator Mapping and Optimizing Design of the Lateral Arm Flap: Clinical Trial

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05718635

Enrollment

Registered

2023-02-08

Start date

2020-10-01

Completion date

2023-06-30

Last updated

2023-03-28

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

Conditions

Coverage of Soft Tissue Defects

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.

Interventions

DIAGNOSTIC_TESTcoloured duplex

colored duplex to locate numbers sites and size of perforators.

PROCEDUREsupra facial dissection

flap raising in supra facial plane

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

16 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* adult patients

Exclusion criteria

* children injury to pedicle

Design outcomes

Primary

Measure	Time frame	Description
numbers of perforators	two years	numbers of perforators in the flap
site of perforators	two years	distance from lateral humeral epicondyle in CM
Size of perforators	two years	size in millimeter

Countries

Egypt

Contacts

Primary ContactOSAMA ELBANNA, MD.

osamaelbanna@aswu.edu.eg021067076234

Outcome results

None listed

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