- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06186362
Results of Distal Clavicle Graft in Shoulder Dislocation Clavicle Auto Graft in Patient With Recurrent Anterior Shoulder Dislocation
January 3, 2024 updated by: Mostafa Khalaf Mahmoud Mohammed, Al-Azhar University
Clinical and Radiological Results of Distal Clavicle Auto Graft in Patient With Recurrent Anterior Shoulder Dislocation
to evaluate the clinical and radiological Outcome of Distal Clavicle Auto graft in patient with recurrent Shoulder dislocation
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
The glenohumeral joint is the most commonly dislocated joint of the human body,The stability of GH joint relies on a complex network of static and dynamic structures,The anterior labrum plays a key role in antero posterior stability as it deepens the glenoid cavity up to 50% There option for glenoid reconstruction including: Distal Clavicle Auto graft (DCA), proven is a good option to coracoid transfers
Study Type
Observational
Enrollment (Estimated)
30
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: Hosam Elsayed Abd-Elzaher, Lecturer
- Phone Number: +201008832805
- Email: Hosamortho@gmail.com
Study Contact Backup
- Name: Mohammed Mousa Mohammed, Assistant Professor
- Phone Number: +201009092327
- Email: MohamedMahmoud.2244@azhar.edu.eg
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
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Range of motion "ROM" (Forward flexion, external rotation, internal rotation) Preoperative and postoperative ROM .
Rowe score, Visual analogue score (VAS).
Secondary outcomes postoperative complications will be evaluated.
Description
Inclusion Criteria:
- Recurrent Traumatic anterior shoulder dislocation (≥ 3 times).
Exclusion Criteria:
.On-track Hill-Sachs lesion. .Multi directional instability.
- Voluntary dislocation.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Row score
Time Frame: At 2 months, 6 months post operative
|
Rang of motion
|
At 2 months, 6 months post operative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
January 1, 2024
Primary Completion (Estimated)
January 1, 2025
Study Completion (Estimated)
January 1, 2025
Study Registration Dates
First Submitted
November 20, 2023
First Submitted That Met QC Criteria
December 27, 2023
First Posted (Actual)
January 2, 2024
Study Record Updates
Last Update Posted (Actual)
January 5, 2024
Last Update Submitted That Met QC Criteria
January 3, 2024
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DCRSD
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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