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

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

      • Istanbul, Turkey, 34450
        • Istanbul University Faculty of Medicine Sports Medicine Department

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
Ultrasound shear-wave elastography

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
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.

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

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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