A study of the efficacy of knee alcohol block for the treatment of knee arthrosis pai
Phase 2
Recruiting
- Conditions
- Gonarthrosis [knee arthrosis]Chronic PainR52.1
- Registration Number
- RBR-2myky3
- Lead Sponsor
- niversidade Federal de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Aged over 18 years. With knee pain for more than six months without improvement with clinical treatment and clinical and imaging diagnosis (radiography) of knee osteoarthritis with moderate pain intensity (pain greater than 4 by numerical scale).
Exclusion Criteria
Patients with cognitive impairment or psychiatric illness or other causes of knee pain (trauma; complex regional pain syndrome; prosthesis); infection at the puncture site; coagulopathy; anticoagulant use will be excluded.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hope we have reduction of pain intensity,Patients will be assessed for pain intensity using a numerical scale from zero to 10 before the block and 15 days, 1, 3 and 6 months after the block; joint movement angle before the block and 1 and 6 months after the block; and WOMAC scale before the block and 15 days, 1, 3 and 6 months after the block.
- Secondary Outcome Measures
Name Time Method Hope we have increased pain-free time, Patients will be assessed for pain intensity using a numerical scale from zero to 10 before the block and 15 days, 1, 3 and 6 months after the block; joint movement angle before the block and 1 and 6 months after the block; and WOMAC scale before the block and 15 days, 1, 3 and 6 months after the block.;A reduction in the use of rescue medications is expected, being assessed by the use of rescue in later assessments.