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

Patellofemoral Joint Clinical Trial

— NPF  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02762630
• Other study ID #: STUDY00000568
• Status: Completed
• Phase: N/A
• First received: May 3, 2016
• Last updated: April 26, 2017
• Start date: July 2016
• Est. completion date: September 2016

Study information

• Verified date: April 2017
• Source: State University of New York at Buffalo
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: September 2016
• Est. primary completion date: September 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Patellofemoral Joint

Intervention

Device:
• Carestream Health Inc. weight bearing cone beam CT scanner

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
State University of New York at Buffalo

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tibial tubercle-trochlear groove (TT-TG) offset distance (mm)		1 day