Dexmedetomidine (10 µg) versus Fentanyl (25 µg) as adjuvants to hyperbaric Bupivacaine for unilateral spinal anesthesia in lower limb orthopedic surgeries
Not Applicable
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202209726231234
- Lead Sponsor
- faculty of medicine Ain Shams University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 54
Inclusion Criteria
Age =21 years and <65 years.
-ASA grade I and II
-both sexes
-Patients undergoing elective orthopedic surgeries of lower limb.
Exclusion Criteria
-Any patient who has history of heart failure (NYHA class ?,?), neuropathy , uncontrolled hypertension, drug abuse, or allergy to the study drugs or has any contraindication of spinal anesthesia
-Patients who can't be placed in a lateral position (e.g., due to pelvis fracture)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method is to measure the time taken for the patient to rescue analgesia<br> <br>
- Secondary Outcome Measures
Name Time Method is to measure :<br> <br>•Time from injection to highest sensory level<br>•Time to two segment regression from the highest sensory level<br>•Time for sensory regression to S1 from highest sensory level<br>• Time from injection to Bromage ?<br>•Time to regression to Bromage 0<br>•Side effects like nausea, vomiting, shivering or respiratory depression for 4 hours after performing spinal anesthesia<br>•Sedation level will be assessed using modified Ramsay scale<br>