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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06199583
Other study ID # IstanbulU-SportsMedicine
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 17, 2020
Est. completion date December 31, 2020

Study information

Verified date December 2023
Source Istanbul University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date December 31, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 17 Years to 35 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Shear-wave elastography
Ultrasound shear-wave elastography

Locations

Country Name City State
Turkey Istanbul University Faculty of Medicine Sports Medicine Department Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shear-wave elastography Ultrasound shear-wave elastography Through study completion, an average of 3 months
Primary Ultrasound Tendon thickness, hypoechoic region, power doppler Through study completion, an average of 3 months
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