Knee Osteoarthritis Clinical Trial
Official title:
Three Needles Approach... A New Technique of Genicular Nerve Radio-frequency Ablation for Pain Relief in Advanced Knee Osteoarthritis
Verified date | August 2018 |
Source | Minia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study is designed to evaluate and compare the efficacy of three needles approach as a new
technique in radiofrequency neurotomy of genicular nerve versus the traditional single needle
approach as a treatment of advanced knee osteoarthritic pain. Primary outcome:
1. Pain intensity via the visual analogue score (VAS).
2. Function and pain via the Oxford Knee Score. Evaluated after 6 months of the procedure
Secondary outcome:
1. Failure rate.
2. Incidence of any complication.
3. Total analgesic requirement during the period of follow up.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | November 2018 |
Est. primary completion date | August 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 35 Years to 85 Years |
Eligibility |
Inclusion Criteria: - 1- Age 35-85 years old 2- Patients with stage 3 or higher OA-related radiological changes based on Kellgren-Lawrence (K/L) rating scale 3- Knee pain for at least 3 months 4-Patients are clinically unresponsive to conservative treatment modalities (physical therapy and rehabilitation practices, orally administered analgesics and anti-inflammatory drugs). Exclusion Criteria: - 1- Patients with other causes of pain as radiculopathy, neurological disorders or intermittent claudication. 2- Previous knee trauma. 3- Previous knee surgery. 4- Patients received intra-articular injection during the previous three months. 5- Acute knee pain. 6- Crystal arthropathy. 7- Joint effusion. 8- Serious neurological or psychiatric disorders. 9- On anticoagulant medication. 10- Any other connective tissue disorder that affects the knee joint. 11- skin infection at the site of injection. 12-patient refusal. |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Medicine, minia university | Minya |
Lead Sponsor | Collaborator |
---|---|
Alaa Fouli Gaber Ebrahim |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual analogue score | Pain intensity via the visual analogue score (VAS). | 6 months after the procedure | |
Primary | Oxford knee score | Follow up of pain and function via the Oxford knee score | 6 months after the procedure | |
Secondary | Failure rate | Persistence of pain after the procedure | 6 months after the procedure | |
Secondary | Incidence of complication | Any infection, heamatoma | 6 months after the procedure |
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