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NCT01905358 · ClinicalTrials.gov registry record
The Knee Usual Care Evaluation Study
A clinical trial, sponsored by Hospital for Special Surgery, New York.
- Terminated
- Registry status
- 906
- Enrollment target
NCT01905358: Clinical Trial study, sponsored by Hospital for Special Surgery, New York.
NCT01905358 is a clinical trial that was terminated before completion, run by Hospital for Special Surgery, New York. The registered enrollment target is 906 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01905358 was terminated before completion, sponsored by Hospital for Special Surgery, New York.
- TERMINATED
- Registry status
- 906 participants
- Enrollment target
Study Summary
The purpose of this prospective data collection is to track patients who are treated at HSS who are confirmed with knee osteoarthritis. The registry will collect prospective patient related and functional outcomes (including use of assistive devices), medication use and imaging data on patients with confirmed osteoarthritis, and the effect of different medical interventions that include PRP, Synvisc / Orthovisc /Euflexxa, bracing, suggested exercises, supplements, and diet. Information from the data collection will be used to compare outcomes of non-surgical alternatives with the end point being knee arthroplasty. The information results will enhance our knowledge of the long-term efficacy and effectiveness of non-surgical interventions intended to treat the progression of osteoarthritis. Hypotheses: * Different non-surgical interventions such as PRP, Synvisc®, Orthrovisc®, Euflexxa, bracing, physical therapy, and a prescribed combination of exercise, diet, and supplements will demonstrate statistically significant differences in patient pain and functional outcomes compared to usual interventions including use of NSAIDs, corticosteroid injections, and use of assistive devices such as canes. * Non-operative interventions for knee osteoarthritis will be associated with different rates of breakdown of articular cartilage and different rates of progression of osteoarthritis as evidenced by MRI or joint space narrowing on standing knee films? * Education about available non-operative treatment methods may change time the end point of total or partial knee replacement for patients with knee osteoarthritis of varying severity. * Different non-operative interventions will be associated with different times to total or partial knee arthroplasty in patient with knee osteoarthritis of similar severity. * An electronic data capture system (EDC) for osteoarthritis patients will improve patient care and patient outcomes.
Primary Outcome
Change is being assessed.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 906 participants |
| Start Date | 2013-07 |
| Est. Completion | 2014-03-21 |
Why NCT01905358 stopped before completion
NCT01905358 is an observational study that tracks outcomes without assigning an intervention. The registered 906 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT01905358 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01905358 about?
NCT01905358 is a clinical study titled "The Knee Usual Care Evaluation Study". The purpose of this prospective data collection is to track patients who are treated at HSS who are confirmed with knee osteoarthritis. The registry will collect prospective patient related and functional outcomes (including use of assistive devices), medication use and imaging data on patients with...
What is the current status of trial NCT01905358?
This trial is currently terminated. The enrollment target is 906 participants. The study started on 2013-07. Estimated completion is 2014-03-21.
Who is sponsoring clinical trial NCT01905358?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
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