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Clinical Trials in Turkey / NCT07659899
Active, not recruiting Observational

Anterior Knee Pain and Patellar Tendon Elasticity After Infrapatellar Tendon-Split Tibial Intramedullary Nailing

NCT07659899 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-12-05
Last updated
2026-08-26

Condition(s) studied

Anterior Knee PainPatellar Tendon DisorderTibial Shaft Fractures

Investigational drug(s) / intervention(s)

Infrapatellar tendon-split tibial intramedullary nailingShear-wave ultrasound elastography

Infrapatellar tendon-split tibial intramedullary nailing: Standard-of-care tibial intramedullary nailing performed through an infrapatellar longitudinal patellar tendon split approach. The procedure is not assigned by the protocol; only patients undergoing this routine surgical approach are observed.

Shear-wave ultrasound elastography: Non-invasive shear-wave ultrasound elastography of the patellar tendon performed at predefined study visits using a standardized imaging protocol.

Study summary

This prospective single-center observational cohort study will evaluate the relationship between anterior knee pain and patellar tendon elasticity after infrapatellar tendon-split tibial intramedullary nailing. Adult patients undergoing standard tibial intramedullary nailing through an infrapatellar tendon-split approach will be enrolled after ethics approval. Patellar tendon elasticity will be assessed using shear-wave ultrasound elastography before surgery and during follow-up at 6 weeks, 3 months, and 6 months. Clinical outcomes will include anterior knee pain severity, patellofemoral function, tendon-related symptoms, and knee range of motion. Inter-rater reliability between two independent radiologists will also be evaluated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18 to 65 years * Unilateral tibial shaft or metaphyseal fracture * Planned treatment with infrapatellar tendon-split tibial intramedullary nailing * Ability to complete baseline and follow-up assessments * Written informed consent Exclusion Criteria: * Previous surgery on the same knee * Previous patellar tendon rupture or known patellar tendon disorder * Active inflammatory rheumatologic disease * Chronic systemic corticosteroid therapy or long-term immunosuppressive treatment * Significant peripheral neuropathy or advanced diabetic neuropathy * Bilateral tibial fracture * Additional major lower-extremity injury or surgery affecting assessment * Inability to comply with scheduled follow-up visits

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bagcilar Training and Research Hospital Istanbul Istanbul

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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 NCT07659899 on ClinicalTrials.gov ↗ ← All trials in Turkey