- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06199583
Diagnostic Value of Shear-Wave Elastography for Patellar Tendinopathy
December 29, 2023 updated by: Sergen Devran, Istanbul University
Diagnostic Value of Shear-Wave Elastography for Patellar Tendinopathy in Female Volleyball and Basketball Athletes
To investigate the accuracy of shear-wave elastography (SWE) in diagnosing patellar tendinopathy in female volleyball and basketball players.
In addition, we want to compare different parts of the patellar tendon and investigated the effects of different knee angles.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
67
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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Istanbul, Turkey, 34450
- Istanbul University Faculty of Medicine Sports Medicine Department
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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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
female athletes between the ages of 17-35 playing professional basketball or volleyball.
Description
Inclusion Criteria were:
- being a female athlete between the ages of 17-35 playing professional basketball or volleyball and agreeing to participate in the study
Exclusion Criteria were:
- to have a history of partial or full-thickness patellar tendon tear,
- if they received an injection in or around the patellar tendon within the past 12 months,
- undergone patellar tendon graft repair for anterior cruciate ligament, had a ligament or meniscus operation within the past six months,
- have a chronic disease (such as diabetes, heart disease, or rheumatic disease),
- are actively using oral contraceptives,
- have an active infection in the knee or surrounding tissues
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 |
---|---|
Patellar tendinopathy
Contains athletes with patellar tendinopathy
|
Ultrasound shear-wave elastography
|
Non-patellar tendinopathy
Contains athletes without patellar tendinopathy
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Ultrasound shear-wave elastography
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shear-wave elastography
Time Frame: Through study completion, an average of 3 months
|
Ultrasound shear-wave elastography
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Through study completion, an average of 3 months
|
Ultrasound
Time Frame: Through study completion, an average of 3 months
|
Tendon thickness, hypoechoic region, power doppler
|
Through study completion, an average of 3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
August 17, 2020
Primary Completion (Actual)
November 1, 2020
Study Completion (Actual)
December 31, 2020
Study Registration Dates
First Submitted
December 17, 2023
First Submitted That Met QC Criteria
December 29, 2023
First Posted (Actual)
January 10, 2024
Study Record Updates
Last Update Posted (Actual)
January 10, 2024
Last Update Submitted That Met QC Criteria
December 29, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IstanbulU-SportsMedicine
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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