- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01072760
Kirschner Wire and Pull-out Wire Fixation for the Treatment of Bony Mallet Finger
February 19, 2010 updated by: The Second Hospital of Qinhuangdao
The objective of this report is to describe a new surgical technique for the treatment of bony mallet finger which involves the application of both Kirschner wire and pull-out wire fixation.
It is believed to decrease the risk of the complications.
Study Overview
Detailed Description
From May 2003 to December 2008, we used Kirschner wire and pull-out wire fixation to carry out 54 closed bony mallet finger in 54 patients.
The bony mallet finger was applicated both Kirschner wire and pull-out wire fixation.
Study Type
Interventional
Enrollment (Actual)
54
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Hebei
-
Qinhuangdao, Hebei, China, 066600
- The second Hospital of Qinhuangdao
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- bony mallet finger;
- patient had failed trials of nonsurgical treatment;
- fracture involving more than 1/3 of the joint surface;
- fragment displacement or subluxation of the DIP joint.
Exclusion Criteria:
- tendinous mallet finger;
- success of nonsurgical treatment;
- comminuted fracture;
- fracture involving at or less than 1/3 of the joint surface which could be successfully replaced with nonsurgical treatment.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: K wire
|
Mallet finger treatment
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The digits were assessed for skin necrosis, skin breakdown, infection.
Time Frame: 15 days
|
15 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The patients rated their pain experience by a visual analogue scale. The results were graded by Crawford's criteria.
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sumin Wen, M.D., The second Hospital of Qinhuangdao
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2003
Primary Completion (Actual)
December 1, 2008
Study Completion (Actual)
February 1, 2009
Study Registration Dates
First Submitted
February 12, 2010
First Submitted That Met QC Criteria
February 19, 2010
First Posted (Estimate)
February 22, 2010
Study Record Updates
Last Update Posted (Estimate)
February 22, 2010
Last Update Submitted That Met QC Criteria
February 19, 2010
Last Verified
February 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- QHD201002
- QHD20010201 (Other Identifier: The second hospital of Qinhuangdao)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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