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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04961879
Other study ID # Soh-Med-21-07-09
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 14, 2021
Est. completion date March 2022

Study information

Verified date February 2022
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

objective of this study is To compare reversed cross finger flap with reversed island homo-digital flap in distal dorsal finger defect reconstruction regarding reliability & functional and aesthetic outcomes . comparative study that will be conducted at Plastic surgery department, Sohag university hospital on 30 patients .The population of the study will be patients with distal dorsal digital defects. We will divide the cases into two equal groups: the first are operated with reversed cross-finger flap and the second are operated with reversed island homo-digital flap.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30
Est. completion date March 2022
Est. primary completion date February 2022
Accepts healthy volunteers No
Gender All
Age group 5 Years to 70 Years
Eligibility Inclusion Criteria: - patients with dorsal digital defect distal to distal interphalangeal joint (DIP) joint - defect size ranged from 1 to 2 cm in width and 1-3 cm in length Exclusion Criteria: - chronic heavy smokers, - traumatic injury to the donor site and perforator .

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Reversed Cross Finger Flap
distal dorsal finger defect will be reconstructed by reversed cross finger flap - reversed cross finger flap is a modified cross finger flap harvested from an adjacent finger .
reversed island homo-digital flap
distal dorsal finger defect will be reconstructed by reversed island homo-digital flap - this flap is harvested from the same finger .

Locations

Country Name City State
Egypt Sohag University Sohag

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary difference in range of motion between group 1 and group 2 difference in range of motion between group 1 and group 2 will be measured by manual goniometer in degrees difference in range of motion between group 1 and group 2 will be measured at 4 months postoperative
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