sefulness of combined femoral nerve blockade and tibital nerve block in patients undergoing bilateral knee replacement.
Not Applicable
- Conditions
- Being prepared.
- Registration Number
- JPRN-UMIN000009141
- Lead Sponsor
- Ryoji Iida
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Central or peripheral nerve dysfunction.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method