- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01725893
Percutaneous Tenotomy of the Toe Flexor Tendon is a Simple and Efficient Method in Treating Checkrein Deformity
November 13, 2012 updated by: National Taiwan University Hospital
Checkrein deformity represents a dynamic claw toe deformity.
Surgical intervention is the treatment of choice and many methods have been proposed.
The purpose of this study is to evaluate the outcomes and complications of percutaneous segmental tenotomy of the toe flexor tendons.
Study Overview
Status
Unknown
Conditions
Detailed Description
The investigators reviewed fourteen patients with checkrein deformity who underwent surgery in our hospital between 1993 and 2010.
Five patients received FHL and flexor digitorum longus (FDL) tenolysis at the musculotendinous junction; among them, two also underwent Z-plasty lengthening of the FHL tendon.
Nine patients underwent percutaneous segmental toe flexor tenotomy.
The Hallux Metatarsophalangeal- Interphalangeal Scale (Hallux MTP-IP scale) and Foot and Ankle Outcome Score (FAOS), English version LK1.0 self-explanatory questionnaire were used to evaluate the functional outcomes.
Study Type
Observational
Enrollment (Anticipated)
14
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jin-Tzer Ho, M.D
- Phone Number: 62515 886 2 23123456
- Email: herginger@gmail.com
Study Locations
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-
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Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Jin-Tzer Ho, M.D
- Phone Number: 62515 886 2 23123456
- Email: herginger@gmail.com
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Principal Investigator:
- Pei-Yu Chen, M.D
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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
18 years to 73 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
There were fourteen patients with checkrein deformity who underwent surgery in our hospital between 1993 and 2010.
Description
Inclusion Criteria:
- Patients with checkrein deformity who underwent surgery in our hospital between 1993 and 2010.
Exclusion Criteria:
- Patients who had static or rigid claw toe deformity
- Patients who had claw toe deformity secondary to neuromuscular disease
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
- Observational Models: Case-Only
- Time Perspectives: Retrospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Hong-Nerng Ho, Professor, National Taiwan University Hospital (NTUH) Research Ethics Committee (REC)
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
March 1, 2012
Primary Completion (Anticipated)
January 1, 2013
Study Completion (Anticipated)
March 1, 2013
Study Registration Dates
First Submitted
September 25, 2012
First Submitted That Met QC Criteria
November 13, 2012
First Posted (Estimate)
November 14, 2012
Study Record Updates
Last Update Posted (Estimate)
November 14, 2012
Last Update Submitted That Met QC Criteria
November 13, 2012
Last Verified
November 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201202038RIC
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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