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NCT01726855 Clinical Trial

Prevention of Adhesions Following Flexor Tendon Injury Within Zone II With Vascularized Finger Dorsal Fascial Flap

Tendon Injuries Clinical Trial

Official title:
Prevention of Adhesions Following Flexor Tendon Injury Within Zone II With Vascularized Finger Dorsal Fascial Flap

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01726855
Other study ID # sun_rising
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2010
Est. completion date July 2012

Study information
Verified date November 2012
Source The Second Hospital of Tangshan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study was to report a new method of flexor tendon repair in zone II with combined standard modified Kessler technique and vascularized finger dorsal fascial flap pedicled with dorsal cutaneous branch of proper digital artery ,which is transported to finger volar for placement of a mechanical barrier between flexor digitorum superficialis /profundus tendons. The function outcomes of 14 patients (Group A) with flexor tendon repair in zone II with this new technique were compared with those of 32 patients (Group B) with flexor tendon repair in zone II with standard modified Kessler technique. This new technique may prevent serious adhesions between flexor digitorum superficialis /profundus tendons.

Recruitment information / eligibility
Status Completed
Enrollment 1
Est. completion date July 2012
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients requiring flexor tendon repair or reconstruction within zone? Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• vascularized finger dorsal fascial flap

Locations
Country Name City State
China the Second Hospital of Tangshan Tangshan Hebei

Sponsors (1)
Lead Sponsor Collaborator
The Second Hospital of Tangshan

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary the modified Strickland system 3~12 months
Primary degrees of the maximum active flexion at the distal interphalangeal joint 3~12 months
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