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Clinical Trials in Turkey / NCT07425340
Starting soon Observational

Ultrasound Examination of the VMO in Patellofemoral Pain Syndrome

NCT07425340 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-25
Last updated
2026-02-20

Condition(s) studied

Vastus MedialisUltrasonographicPatello Femoral Pain Syndrome

Study summary

The aim of this study is to examine in detail the ultrasonographic characteristics of the vastus medialis obliquus and vastus medialis longus muscles in individuals with patellofemoral pain syndrome and to compare these findings with those of healthy individuals. It is anticipated that the results obtained will contribute to a better understanding of the muscle-based mechanisms of PFAS and provide a scientific basis for the development of muscle-specific assessment and intervention strategies in physical therapy and rehabilitation practices.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Between the ages of 18 and 65 * Have had localized pain in the front of the knee for at least the past 3 months * Experience pain during activities that require stair climbing, squatting, prolonged sitting, or knee flexion * Have been diagnosed with patellofemoral pain syndrome based on clinical evaluation * Volunteer to participate in the study and sign the informed consent form Exclusion Criteria: * History of previous surgery on the knee joint * History of significant trauma to the knee region within the last 6 months * Diagnosis of meniscus, ligament injuries, knee osteoarthritis, or inflammatory rheumatic disease * Neurological diseases or systemic diseases affecting the musculoskeletal system * Presence of other lower extremity pathologies causing pain at a level that could affect measurements

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hasan Kalyoncu University Gaziantep Şahinbey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07425340 on ClinicalTrials.gov ↗ ← All trials in Turkey