Registry for knee osteoarthritis pain management outcomes
Innovations in Genicular Outcomes Registry
This study is trying to see how well different pain management treatments work for people with knee osteoarthritis and those who have had knee surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Sex | All |
| Sponsor | Pacira Pharmaceuticals, Inc Industry-sponsored |
| Locations | 17 sites (Phoenix, Arizona and 16 other locations) |
| Trial ID | NCT05495334 on ClinicalTrials.gov |
What this trial studies
This registry captures prospective data on patients receiving various pain management therapies for chronic pain due to knee osteoarthritis or those undergoing knee arthroplasty. Treatments may include cryo nerve block, radiofrequency ablation, intra-articular corticosteroids, viscosupplementation, and opioids. The goal is to optimize pain management and assess outcomes related to these interventions. Patients will complete questionnaires via a registry application to provide valuable data on their experiences and treatment effectiveness.
Who should consider this trial
Good fit: Ideal candidates are patients planning to receive treatment for knee osteoarthritis pain within 60 days of screening.
Not a fit: Patients actively enrolled in other investigational trials or planning surgeries on knees other than the target knee may not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of effective pain management strategies for knee osteoarthritis, leading to improved patient outcomes.
How similar studies have performed: Other studies have shown success in capturing patient outcomes through registries, indicating that this approach is promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Planned to receive treatment for knee OA pain including, but not limited to, knee injections, nerve blocking procedures, or knee arthroplasty within 60 days of screening 2. Able to understand the informed consent and assessment questionnaires and have the ability to complete them in the opinion of the investigator 3. Have access to a smartphone or internet access with a computer/tablet to complete the questionnaires using the registry application Exclusion Criteria: 1. Actively enrolled in an investigational trial that would preclude patients from receiving the site's standard of care for knee OA pain or knee arthroplasty recovery protocol 2. Planning to have a surgery other than on the target knee
Where this trial is running
Phoenix, Arizona and 16 other locations
- The MORE Foundation — Phoenix, Arizona, United States (Recruiting)
- Orthopedic Education and Research Institute of So Ca (Hoag) — Irvine, California, United States (Recruiting)
- Cedars-Sinai Medical Center — Los Angeles, California, United States (Recruiting)
- MidState Orthopedics and Sports Medicine — Alexandria, Louisiana, United States (Recruiting)
- Louisiana State University /Ochsner — New Orleans, Louisiana, United States (Recruiting)
- Sinai Hospital of Baltimore — Baltimore, Maryland, United States (Recruiting)
- Henry M Jackson Foundation for the Advancement of Military Medicine/Walter Reed National Military Medical Center — Bethesda, Maryland, United States (Recruiting)
- OrthoNebraska Clinics — Omaha, Nebraska, United States (Recruiting)
- Jersey City Medical Center — Jersey City, New Jersey, United States (Terminated)
- Northwell Health — Garden City, New York, United States (Not_yet_recruiting)
- Genesee Orthopedics and Plastic Surgery (St. Elizabeth Med Center/ Apex Surgical Center) — New Hartford, New York, United States (Completed)
- Blue Nine Systems — Asheville, North Carolina, United States (Terminated)
- Oklahoma Surgical Hospital — Tulsa, Oklahoma, United States (Recruiting)
- Penn Highlands DuBois — DuBois, Pennsylvania, United States (Recruiting)
- University Orthopedics Center — State College, Pennsylvania, United States (Recruiting)
- Campbell Clinic — Germantown, Tennessee, United States (Recruiting)
- University of Utah — Salt Lake City, Utah, United States (Not_yet_recruiting)
Study contacts
- Study coordinator: Kate Fasel, BSN
- Email: IGOR@pacira.com
- Phone: 1-520-490-5355
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.