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OpenTrials
Completed

NCT Number: NCT02762630

Use of a Novel Weight Bearing Cone Beam Computed Tomography (CBCT) Scanner for Imaging of the Patellofemoral Joint

Healthy volunteers will have a weight bearing cone beam CT scan of their knee to assess normal alignment of the knee joint

Completed

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Key information

Conditions

Patellofemoral Joint

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Willing and able to provide written informed consent
  • Be 16 or more years of age
  • Subject is able to be positioned properly in the investigational device and be still during the exam to reduce the potential of motion during the images

Exclusion criteria

  • Have a history of patella instability
  • Have had any type of previous knee surgery
  • Have had a significant fracture of the patellofemoral joint
  • Have a knee ligament injury
  • Are pregnant at the time of screening or become pregnant during the study
  • Have a history of high radiation exposure (i.e., undergone radiation therapy)
  • Non-English speakers

Treatment and study plan

Carestream Health Inc. weight bearing cone beam CT scanner

Device

Primary outcomes

  1. Tibial tubercle-trochlear groove (TT-TG) offset distance (mm)

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

State University of New York at Buffalo

Other

Registry information

Acronym: NPF

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 5, 2016
Registry last updated
Apr 27, 2017

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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