Comparison between Femoral Nerve Anesthesia and Adductor Canal Anesthesia in analgesia and mobility in patients undergoing Revision knee prosthesis surgery randomized controlled clinical trial
Not Applicable
- Conditions
- ArthroplastyE04.555.110.110.115
- Registration Number
- RBR-2n5b5y3
- Lead Sponsor
- Ministério da Saúde
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients undergoing total knee arthroplasty revision surgery; both sexes; older than 18 years; classified by the American Society of Anesthesiology (ASA) as physical status I to III
Exclusion Criteria
Patients with daily consumption of opioids and/or antidepressants; patients in whom it was necessary to perform general anesthesia; patients with neurological and muscular diseases; patients allergic to dipyrone, tramadol and local anesthetics; bedridden and amputated patients; and patients with grade III obesity (BMI > 40)
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assess the intensity of pain, at rest and movement, 24 and 48 hours after surgery
- Secondary Outcome Measures
Name Time Method Quantify opioid consumption 24 and 48 hours postoperatively;Assess the lifting capacity of the operated limb 24 and 48 hours after surgery;Assess the patient's ability to remain in an orthostatic position 24 and 48 hours postoperatively;Assess the ability to walk 24 and 48 hours postoperatively