The PERK Study: Predicting and Evaluating Response to Knee RFA Using fNIRS
- NCT ID
- NCT07835269
- Registry status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Conditions
- Osteo Arthritis of the Knee, Pain
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 30 participants (Estimated).
What is being studied
- Intervention: Ablation Techniques
- Diagnostic test: Genicular Nerve Block
- Intervention: Radiofrequency Ablation
- Procedure: Radiofrequency ablation alone
- Intervention: Radiofrequency Therapy
- Intervention: Surgical Procedures, Operative
- Intervention: Therapeutics
Who may be eligible
- Ages
- 18 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* ≥18 years old
* Have osteoarthritis in either knee
Exclusion Criteria:
* Limited English proficiency or lack of capacity to consent (per clinical judgement)
* Scheduled for knee arthroplasty within next 6 months
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Canada
- Ontario, Canada: 1
Sample of listed locations
- St. Joseph's Hospital London — London, Ontario, Canada — Site recruitment status not specified in the registry data
Study details
- Start date
- October 1, 2026
- Primary completion date
- October 1, 2028
- Completion date
- May 1, 2029
- First posted
- September 22, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07835269
- Registry last updated
- September 22, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07835269 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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