- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01278251
Functional Review of Distal Biceps Re-Insertion
January 14, 2011 updated by: West Penn Allegheny Health System
This study seeks to test the hypothesis that endobutton repair of the ruptured distal biceps successfully restores elbow function.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
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
-
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Pennsylvania
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Pittsburgh, Pennsylvania, United States, 15237
- Allegheny Imaging of McCandless
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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 78 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who have received primary distal biceps repair by Dr. Schmidt.
Description
Inclusion Criteria:
- primary distal biceps repair with endobutton
- at least two years from date of surgery
Exclusion Criteria:
- any ipsilateral wrist, forearm, or elbow condition
- any contraindication to having an MRI
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Endobutton
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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 Registration Dates
First Submitted
January 14, 2011
First Submitted That Met QC Criteria
January 14, 2011
First Posted (Estimate)
January 17, 2011
Study Record Updates
Last Update Posted (Estimate)
January 17, 2011
Last Update Submitted That Met QC Criteria
January 14, 2011
Last Verified
January 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC-4556
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.
Clinical Trials on Distal Biceps Ruptures
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University Hospitals Cleveland Medical CenterWithdrawn
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St. Louis UniversityTerminatedBicep Tendinitis | Biceps; Tenosynovitis | Biceps Tendon DisorderUnited States
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Soft Tissue Regeneration, Inc.TerminatedAcute Ruptures of the Anterior Cruciate LigamentNetherlands
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West Penn Allegheny Health SystemCompleted
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Hadassah Medical OrganizationUnknown
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University of AlbertaCompleted
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University Hospital, Basel, SwitzerlandHospital Fribourg, Switzerland; Hospital Liestal, SwitzerlandCompleted
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University of Colorado, DenverUniversity of Newcastle, AustraliaWithdrawnBicep Tendinitis | Biceps; Tenosynovitis | Bicipital Tendinitis, Left Shoulder | Bicipital Tendinitis, Right Shoulder | Bicipital Tendinitis, Unspecified Shoulder | Biceps Tendon DisorderUnited States
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Contrad Swiss SACompletedLong Head of Biceps RuptureItaly
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Schulthess KlinikCompletedDistal Interphalangeal Arthroplasty | Distal Interphalangeal ArthrodesisSwitzerland
Clinical Trials on Distal Biceps Re-Insertion
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West Penn Allegheny Health SystemCompleted
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Hadassah Medical OrganizationUnknown
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University of MalayaWithdrawn
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PAULO VINICIUS SOARESUnknownMTA | Calcium Hydroxide | Endodontic TreatmentBrazil