- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05194774
Greater Trochanter Epiphysiodesis In Hip Pathology
January 4, 2022 updated by: Muhammed Yasser, Al-Azhar University
Outcomes of The Greater Trochanter Epiphysiodesis In Treatment Of Children With Hip Pathology
One of the most common problems in the treatment of pediatric patients with various disorders of the hip joint is the formation of deformity of the proximal femur, such as abnormal growth of the greater trochanter, which causes it to be positioned high in relation to the femoral head.
This condition is called "relative overgrowth of the greater trochanter" (ROGT).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
20
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: Muhammed Yasser, MD
- Phone Number: 0201061303076
- Email: docmuhammed1@gmail.com
Study Contact Backup
- Name: Amer Alkott, MD
- Phone Number: 01002329851
- Email: amerabomosab@yahoo.com
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
5 years to 10 years (CHILD)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The patients come to the outpatient clinic and underwent clinical and radiological examination will be done , then preparation to surgery by screw
Description
Inclusion Criteria:
- emerging deformities of the proximal femur with a high position of the greater trochanter, in which its apex was located above the center of the femoral head but below its superior pole; changes in the structure of the femoral neck, accompanied by its shortening; functioning growth zone of the greater trochanter at the time of intervention; and patients without surgical treatment history
Exclusion Criteria:
- hip dislocation upon examination; patients with varus deformity of the femoral neck (neck-shaft angle <120°), patients with complications of surgical interventions, trauma, rickets, and rheumatoid arthritis; and patients with neurological disorders and Refusal to participate in this study
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
GT overgrowth group
pediatric patients with greater trochanter overgrowth
|
epiphysiodesis by cortical screw and washer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Radiological measurments
Time Frame: 12 month
|
articulo-trochanteric distance
|
12 month
|
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 (ANTICIPATED)
January 1, 2022
Primary Completion (ANTICIPATED)
January 1, 2023
Study Completion (ANTICIPATED)
January 1, 2024
Study Registration Dates
First Submitted
January 4, 2022
First Submitted That Met QC Criteria
January 4, 2022
First Posted (ACTUAL)
January 18, 2022
Study Record Updates
Last Update Posted (ACTUAL)
January 18, 2022
Last Update Submitted That Met QC Criteria
January 4, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GTE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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