Perforator Mapping and Optimizing Design of the Lateral Arm Flap

NCT ID: NCT05718635

Last Updated: 2023-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-01

Study Completion Date

2023-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coverage of Soft Tissue Defects

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

patients candidate for lateral arm flap

Group Type EXPERIMENTAL

coloured duplex

Intervention Type DIAGNOSTIC_TEST

colored duplex to locate numbers sites and size of perforators.

supra facial dissection

Intervention Type PROCEDURE

flap raising in supra facial plane

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

coloured duplex

colored duplex to locate numbers sites and size of perforators.

Intervention Type DIAGNOSTIC_TEST

supra facial dissection

flap raising in supra facial plane

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* adult patients

Exclusion Criteria

* children injury to pedicle
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Aswan University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Osama Hassan Elbanna

Associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of Medicine

Aswān, , Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

OSAMA ELBANNA, MD.

Role: CONTACT

021067076234

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

OSAMA ELBANNA, MD

Role: primary

021067076234

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AswanU

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.