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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04690543
Other study ID # ANaseem
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 2021
Est. completion date July 2021

Study information

Verified date December 2020
Source Dow University of Health Sciences
Contact Aiman Naseem
Phone 03215621936
Email aiman.naseem1@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the purpose of this study is to compare the gain in length after postburn contracture release using two different techniques, the more commonly practised z - plasty and relatively newer technique, square flap


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date July 2021
Est. primary completion date July 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 50 Years
Eligibility Inclusion Criteria:- • Both genders. - Joints supple. - Linear contracture bands. - Age between 5years to 50 years. - Surrounding non scarred skin. - Contractures of axilla, cubital fossa, popliteal fossa and digits. Exclusion Criteria: - Deep burns. - Joint contractures. - Surrounding skin scarred. - Broad, irregular contracture. - Neck, Perineal, wrist or toe contractures

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
z-plasty
Z-plasty: It will be defined as a local transposition flap that will be used to improve the functional and cosmetic appearance of scars. It will be involved creating two triangular flaps of equal dimensions that will be transposed.
square flap
Square flap: It will be defined as is another local transposition flap which will be used for release of contractures. Square will be marked on one side of the contracture, and two triangles will be marked on the other side, with the length of all the flaps equal, which will be then transposed.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Dow University of Health Sciences

Outcome

Type Measure Description Time frame Safety issue
Primary gain in length calculation of the gain in length achieved after the release of post burn contrature 3 weeks
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