A randomized controlled trial compairing femoral nerve block and periarticular multimodal drug injection for anterior cruciate ligament reconstructio
Not Applicable
- Conditions
- Anterior cruciate ligament injury
- Registration Number
- JPRN-UMIN000014001
- Lead Sponsor
- Hyogo College of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
The exclusion criteria were revision ACL reconstruction, ACL reconstruction with bone-patellar tendon-bone graft, combined with other ligament reconstruction, combined with high tibial osteotomy, allergy to one of the study drugs, regular narcotic use, renal insufficiency, severe obesity (BMI > 35) and ECG abnormalities at rest.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative visual analog scale score at rest 24 hours after surgery.
- Secondary Outcome Measures
Name Time Method Post operative visual analog scale score at rest until 14 days after surgery. The postoperative VAS scores for patient satisfaction with pain management until 3 days after surgery. The total amount of opioid consumption after surgery. Post operative complication.