Application of Combined Lumbar Plexus and Sciatic Nerve Block
- Conditions
- Anesthesia
- Interventions
- Procedure: Nerve blockProcedure: Combined spinal and epidural anesthesia
- Registration Number
- NCT02084368
- Lead Sponsor
- Guangzhou General Hospital of Guangzhou Military Command
- Brief Summary
The research is to study the effectiveness and safety of combined lumbar plexus and sciatic nerve block by the guide of peripheral nerve stimulator (PNS) in unilateral knee replacement.There have be some papers which supported that combined lumbar plexus and sciatic nerve block may be more suitable for the old men.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
- Patients of American Association of anesthetists(ASA)Grade 1、2 or 3
- Aged between 18 and 85 years
- Undergoing elective total knee replacement.
- Mental illness can not match
- Nerve block, epidural anesthesia contraindicated
- People who have Slow-type arrhythmias
- History of chronic headaches and long-term use of analgesic drugs
- People who were postoperative consciousness, language or hearing impaired
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Nerve block Nerve block Patients in this group were assigned to receive lumbar plexus block and sciatic nerve block guided by PNS. combined spinal and epidural anesthesia Combined spinal and epidural anesthesia Combined spinal and epidural anesthesia were performed in patients of this group. Nerve block Ropivacaine Patients in this group were assigned to receive lumbar plexus block and sciatic nerve block guided by PNS. combined spinal and epidural anesthesia Bupivacaine Combined spinal and epidural anesthesia were performed in patients of this group.
- Primary Outcome Measures
Name Time Method Maintenance time of sensory and motor nerve block up to 24h after operation from the end of injection of local anesthetic drug up to 24h after operation
- Secondary Outcome Measures
Name Time Method The change of hemodynamics 0, 5, 10, 20, 30, 60 min after injection the changes of SBP and DBP at 0, 5, 10, 20, 30, 60 min after injection
Trial Locations
- Locations (1)
Guangzhou Military Region General Hospital, Department of Anesthesiology
🇨🇳Guangzhou, Guangdong, China