Innovations in Genicular Outcomes Registry (iGOR)

Pacira

Status: Enrolling

Conditions: Knee Osteoarthritis

Treatments: Procedure: Treatment for Knee OA

Study type: Observational

Funder types: Industry

Identifiers

NCT05495334

IOV-REG-001

Details and patient eligibility

About

The registry will capture prospective data on patients receiving pain management for chronic pain due to knee osteoarthritis (OA) or pain optimization for knee arthroplasty due to knee OA. The OA pain therapies may include cryo nerve block, radiofrequency ablation (RFA), intra-articular (IA) corticosteroids, viscosupplementation, opioids, and others (e.g., non-steroidal anti-inflammatory drugs [NSAIDs]).

Enrollment: 10,000 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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

Trial design

10,000 participants in 1 patient group

All participants

Description:

Eligible and enrolled subjects with knee OA pain who require treatment on the target knee as a part of pain management.

Treatment:

Procedure: Treatment for Knee OA