Status:
TERMINATED
Cooled Versus Conventional Genicular Radiofrequency Ablation for Chronic Knee Pain
Lead Sponsor:
Henry Ford Health System
Conditions:
Chronic Knee Pain
Eligibility:
All Genders
18+ years
Brief Summary
This prospective observational study seeks to compare pain relief and disability following cooled radiofrequency ablation (Coolief) versus conventional genicular nerve ablation in patients with chroni...
Detailed Description
This prospective observational study seeks to compare pain relief at 1 month, 3 months and 6 months following cooled radiofrequency ablation vs conventional genicular nerve ablation in patients with c...
Eligibility Criteria
Inclusion
- Adult male or female (above age of 18)
- Diagnosed with chronic knee osteoarthritis or post Total Knee Arthroscopy or post Total Knee Replacement Pain
- More than 3 months of knee pain
- Scheduled for Genicular Knee ablation (Cooled or conventional ablation)
- Had previous intra articular injection (steroids or Hyaluronic acids) if not a post-surgical knee pain patient
- Achieved minimum 50% relief from genicular block x 2
- Numeric Rating Scale Score of 4 or greater
- Kellgren-Lawrence Knee Osteoarthritis Grade 2 or greater (in non post-surgical patients)
Exclusion
- Pregnant adult female
- Patient fully anticoagulated
- Antiplatelet Use
- History of Clotting Disorder
- Refusal to participate
- Focal neurologic deficits
- Cognitive deficits
- History of Bone Cancer
- Mental Health Illness which causes instability
- Previous Knee radiofrequency ablation
- Active Infection
- Allergy to Medications Administered
Key Trial Info
Start Date :
July 11 2020
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 24 2020
Estimated Enrollment :
1 Patients enrolled
Trial Details
Trial ID
NCT04275128
Start Date
July 11 2020
End Date
September 24 2020
Last Update
September 28 2020
Active Locations (1)
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1
Henry Ford Health System
Detroit, Michigan, United States, 48201