Understanding Knee Pain and Osteoarthritis with WBCT

This observational study is looking at the connection between the shape of your kneecap joint (patellofemoral joint, or PFJ) and knee pain, including patellofemoral pain (often called "runner's knee") and knee osteoarthritis (OA). Researchers will use a special type of X-ray called a WBCT (weight-bearing computed tomography) to get detailed 3D images of your knee while you're standing. This helps them see how your kneecap moves under normal conditions. The goal is to understand if certain shapes of the PFJ are linked to specific knee symptoms. This knowledge could help doctors better understand and treat the causes of your knee pain. The study plans to enroll 36 participants and is currently unclear on its recruitment status.

Study design
This is an observational study, meaning it looks at existing conditions without giving new treatments. It plans to include 36 participants.
What's involved
You would have images of your knee taken using a WBCT scan. This scan provides a 3D view of your kneecap joint while bearing weight.
Compensation
Not stated in the trial record.
Follow-up
Measurements for the main goals of the study will be taken from enrollment to the end of the study, which is 1 day.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07472088

Assessing the Association Between WBCT PFJ Morphological Metrics and Knee Symptoms

Recruiting
Not specifiedAges 18+Observational
University of Kansas Medical Center
~36 participants
Updated 2026-05-07 on ClinicalTrials.gov
What's tested:WBCT

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
TT-TG
Measured over From enrollment to end of study (1 day)
+2 more outcomes measured
Knee Osteoarthritis
Patellofemoral Pain (PFPS)

NCT07472088

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Kansas Medical Center

    Kansas City, Kansasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Neil A Segal, MD, MS · PRINCIPAL_INVESTIGATOR · University of Kansas Medical Center

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Eligibility criteria

Inclusion

Age ≥ 18
Knee pain, falling into either of the two groups, i.e., PFJ pain (pain only in the anterior region of the knee) or symptomatic knee OA (pain in any other area of the knee, including the anterior region)

Exclusion

Bilateral total knee arthroplasty
Pregnant
Unable to stand safely for 2 minutes with support
Any condition that the investigator identifies as inappropriate for participation (e.g., unable to participant in consent process, unsafe to stand on WBCT platform, etc.)
  • TT-TGFrom enrollment to end of study (1 day)

    Tibial Tuberosity - Trochlear Grove (TT-TG) will be measured on 3D WBCT knee images acquired at 0° and 20±5° of knee flexion.

  • reTRFFrom enrollment to end of study (1 day)

    Relative external tibiofemoral rotation (reTFR) will be measured on 3D WBCT knee images acquired at 0° and 20±5° of knee flexion.

  • Congruence AngleFrom enrollment to end of study (1 day)

    Congruence angle will be measured on 3D WBCT knee images acquired at 20±5° of knee flexion.