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NCT Number: NCT07659899

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

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.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Bagcilar Training and Research Hospital

Istanbul, 34320, Turkey (Türkiye)

About this study

Anterior knee pain is a frequent complaint after tibial intramedullary nailing, but the role of patellar tendon biomechanical changes remains unclear. The infrapatellar tendon-split approach may lead to tendon healing, remodeling, and fibrosis, which could alter tendon elasticity and contribute to persistent pain and functional limitation. This study aims to prospectively investigate whether changes in patellar tendon elasticity are associated with anterior knee pain after infrapatellar tendon-split tibial intramedullary nailing.

This is a prospective, single-center, non-interventional observational cohort study. Adult patients aged 18 to 65 years with unilateral tibial shaft or metaphyseal fractures treated with standard infrapatellar tendon-split tibial intramedullary nailing will be enrolled consecutively after institutional ethics approval. Only patients enrolled after ethics approval will be included in the registered cohort.

Patellar tendon elasticity will be measured using shear-wave ultrasound elastography at four predefined time points: preoperatively, 6 weeks, 3 months, and 6 months postoperatively. Ultrasound assessments will be performed according to a standardized protocol by two independent radiologists, and inter-rater reliability will be assessed. Additional ultrasound parameters will include tendon thickness on B-mode imaging and Doppler neovascularization.

Clinical outcomes will include anterior knee pain assessed with a visual analog scale, patellofemoral function assessed with the Kujala Anterior Knee Pain Scale, tendon-related symptoms assessed with the VISA-P questionnaire, pressure pain sensitivity, and active knee range of motion. The primary objective is to determine whether change in patellar tendon elasticity is associated with anterior knee pain at 6 months. Secondary objectives are to examine associations between tendon elasticity and functional scores, range of motion, tendon thickness, Doppler findings, and inter-rater measurement reliability.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Infrapatellar tendon-split tibial intramedullary nailing

Procedure

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

Diagnostic Test

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

Primary outcomes

  1. Change in patellar tendon elasticity from baseline to 6 months

    Time frame: Preoperative baseline and 6 months postoperatively

    Patellar tendon elasticity measured by shear-wave ultrasound elastography in kilopascals. The primary analysis will assess the longitudinal change from baseline to 6 months.

Secondary outcomes

  1. Change in patellar tendon elasticity from baseline to 3 months

    Time frame: Preoperative baseline and 3 months postoperatively

    Change in patellar tendon elasticity measured by shear-wave ultrasound elastography.

  2. Anterior knee pain severity

    Time frame: Baseline and postoperative 6 weeks, 3 months, and 6 months

    Anterior knee pain severity will be assessed using the Visual Analog Scale. The Visual Analog Scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate worse anterior knee pain.

  3. Patellofemoral function

    Time frame: Preoperative baseline, 3 months, and 6 months

    Patellofemoral function will be assessed using the Kujala Anterior Knee Pain Scale. The scale ranges from 0 to 100 points, with higher scores indicating better patellofemoral function and fewer anterior knee symptoms.

  4. Patellar Tendon-Related Symptoms and Function

    Time frame: Preoperative baseline, 3 months, and 6 months

    Patellar tendon-related symptoms and function will be assessed using the Victorian Institute of Sport Assessment-Patella questionnaire. The questionnaire ranges from 0 to 100 points, with higher scores indicating fewer patellar tendon-related symptoms and better function

  5. Active knee range of motion

    Time frame: Preoperative baseline, 6 weeks, 3 months, and 6 months

    Active knee flexion and extension lag measured with a goniometer.

  6. Patellar tendon thickness

    Time frame: Preoperative baseline, 6 weeks, 3 months, and 6 months

    Patellar tendon thickness measured on B-mode ultrasound.

  7. Doppler neovascularization

    Time frame: Preoperative baseline, 6 weeks, 3 months, and 6 months

    Semiquantitative Doppler neovascularization score.

  8. Pressure Pain Sensitivity

    Time frame: 6 weeks, 3 months, and 6 months

    Pressure pain sensitivity will be assessed by recording pain intensity during a standardized pressure pain assessment using the Visual Analog Scale. The Visual Analog Scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pressure pain sensitivity.

  9. Inter-rater reliability of shear-wave elastography measurements

    Time frame: Baseline, 6 weeks, 3 months, and 6 months

    Agreement between two independent radiologists assessed using intraclass correlation coefficients.

Sponsors and collaborators

Lead sponsor

Bagcilar Training and Research Hospital

Other Gov

Registry information

Official study title

Relationship Between Anterior Knee Pain and Patellar Tendon Elasticity After Infrapatellar Tendon-Split Tibial Intramedullary Nailing: A Prospective Cohort Study Using Shear-Wave Ultrasound Elastography

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 22, 2026
Registry last updated
Jun 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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