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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01019811
Other study ID # STS-5xb-86
Secondary ID
Status Completed
Phase N/A
First received November 20, 2009
Last updated November 23, 2009
Start date May 2001
Est. completion date May 2008

Study information

Verified date November 2009
Source The Second Hospital of Tangshan
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to introduce a new operative technique for reconstruction of fingertip degloving injury.


Description:

Incidence of fingertip degloving injury is common and can result in functional morbidity. A cross-finger flap based on the dorsal branch artery (DBA) including sensory nerve is a useful reconstructive technique.In our modification, the innervated sensory flap is vascularized by the DBA, both its pedicle is narrow and its coverage is extended, the projecting tip of exposed distal phalanx of adjacent digits therefore can be wrapped.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date May 2008
Est. primary completion date May 2006
Accepts healthy volunteers No
Gender Both
Age group 12 Years to 59 Years
Eligibility Inclusion Criteria:

- the fingertip degloving injury including the thumb;

- age between 12 and 59 years;

- no life-threatening associated injuries.

Exclusion Criteria:

- age greater than 60 years;

- smoking;

- Dupuytren's contracture;

- peripheral arterial disease and other vascular disorders.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
The innervated sensory cross-finger flap
The innervated sensory cross-finger flap is a modified method for repair fingertip degloving injury

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 static 2-point discrimination test and the range of motion are used for evaluation of outcomes at least 4 months No
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