KineSpring® System Patient Preference Study
Completed
- Conditions
- Osteoarthritis of the Knee
- Registration Number
- NCT02934672
- Lead Sponsor
- Moximed
- Brief Summary
The primary objectives of the survey are to obtain patient preference information that can be useful during the benefit-risk assessment of the KineSpring System.
- Detailed Description
Well-established, quantitative research methods were employed to understand the relative importance of effectiveness, safety, and other characteristics of orthopedic surgical treatments and develop a benefit-risk model to inform regulatory decision making.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 323
Inclusion Criteria
- Males and females aged 25 - 80 years
- Diagnosed with osteoarthritis in the knee
- Experience pain in the knee of greater than or equal to a "4" on a "0 - 10" scale, where 0 means not at all painful and 10 means extremely painful
- Experience knee pain at least once a week
- Previously failed non-surgical treatments for knee OA pain
- Pass a security screen
Exclusion Criteria
- Do not suffer or has not been diagnosed with knee osteoarthritis
- Has had knee surgical intervention involving an implant or a prosthesis (i.e. total knee replacement, unicompartmental knee arthroplasty, high tibial osteotomy)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient preferences for knee osteoarthritis surgical procedures At time of survey Patient preference for knee osteoarthritis surgeries
- Secondary Outcome Measures
Name Time Method