Evaluation of low dose Intrathecal Bupivacaine with dexmedetomidine
Phase 2
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202403633859291
- Lead Sponsor
- mansoura university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
elderly patients (>65 years)
either gender
American Society of Anesthesiologists status I and II
patients undergoing proximal femoral fractures fixation under spinal anesthesia
Exclusion Criteria
age less than 65 years
American Society of Anesthesiologists (ASA) physical status class III or more
Contraindication to spinal anaesthesia:
peripheral neuropathy
coagulopathy
spinal deformity infection at the injection site
known hypersensitivity to bupivacaine or dexmedetomidine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method time to 1st dose rescue analgesia
- Secondary Outcome Measures
Name Time Method sensory level block, two segment regression, hemodynamic stability and dose of vasopressors required intraoperative;The total number of rescue analgesic doses required in 24 h postoperative, postoperative analgesia using numerical rating scale NRS, postoperative analgesic duration