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NCT04275128 · ClinicalTrials.gov registry record
Cooled Versus Conventional Genicular Radiofrequency Ablation for Chronic Knee Pain
A clinical trial, sponsored by Henry Ford Health System.
- Terminated
- Registry status
- 1
- Enrollment target
NCT04275128 is a clinical trial that was terminated before completion, run by Henry Ford Health System. The registered enrollment target is 1 participants.
The verdict
NCT04275128 was terminated before completion, sponsored by Henry Ford Health System.
- TERMINATED
- Registry status
- 1 participants
- Enrollment target
Study 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 chronic knee pain. Patients' NRS for pain, WOMAC, and ODI score at baseline and 1, 3 and 6 months after treatment will be used to evaluate whether Coolief is more effective at reducing disability and improving pain relief.
Interventions
- DEVICE Cooled radiofrequency ablation
- DEVICE Conventional radiofrequency ablation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1 participants |
| Start Date | 2020-07-11 |
| Est. Completion | 2020-09-24 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04275128
The ClinicalTrials.gov registry entry for NCT04275128 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Cooled radiofrequency ablation is the first listed.
NCT04275128 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04275128 about?
NCT04275128 is a clinical study titled "Cooled Versus Conventional Genicular Radiofrequency Ablation for Chronic Knee Pain". This prospective observational study seeks to compare pain relief and disability following cooled radiofrequency ablation (Coolief) versus conventional genicular nerve ablation in patients with chronic knee pain. Patients' NRS for pain, WOMAC, and ODI score at baseline and 1, 3 and 6 months after tr...
What is the current status of trial NCT04275128?
This trial is currently terminated. The enrollment target is 1 participants. The study started on 2020-07-11. Estimated completion is 2020-09-24.
What interventions are being tested in trial NCT04275128?
The interventions under investigation include: Cooled radiofrequency ablation (DEVICE), Conventional radiofrequency ablation (DEVICE).
Who is sponsoring clinical trial NCT04275128?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
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