Comparison of postoperative analgesia and side effects of ropivacine and bupivacaine by continous epidural analgesia after lower extremity orthopedic surgery
Phase 1
- Conditions
- Analgesia after lower extremity orthopedic sugery.Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate
- Registration Number
- IRCT201202277984N4
- Lead Sponsor
- Research Deputy, Tehran University of Medical Sciences (TUMS)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
age between 18-65 years old; ASA I and II and scheduled for lower extremity orthopedic surgery.
Exclusion criteria: Opioid adiction or abuse; lower extremity muscle weakness; hypersensitivity to opioids; patient refusal at any time during projetc and coagulopathy or anticoagulant therapy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: data were recorded at immediate before pump filling, 6, 12, 24, 36, and 48 hours later. Method of measurement: Visual Analog Scale (VAS).
- Secondary Outcome Measures
Name Time Method Motor blockade. Timepoint: data were recorded at immediate before pump filling, 6, 12, 24, 36, and 48 hours later. Method of measurement: Bromage scale.