To compare efficacy and safety of hyperbaric ropivacaine with hyperbaric bupivacaine for spinal anesthesia in patients undergoing lower limb orthopedic surgeries
Phase 4
- Conditions
- Health Condition 1: 7- Osteopathic
- Registration Number
- CTRI/2022/06/043286
- Lead Sponsor
- Government medical college haldwani
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Males or females
1. 18-70 years of age
2. American society of anesthesiologists (ASA) grade 1 or 2
3. Orthopedic lower limb surgeries
4. Under Spinal anesthesia
Exclusion Criteria
1.Patients not in the desired age group
2.ASA grade >2
3.Coagulopathy
4.Patients with known allergy to study drugs
5.Patient refusal for spinal anesthesia
6.Patient who require epidural along with spinal anesthesia
7.Patient requiring conversion of spinal to general anesthesia
8.Expected duration of surgery more than 3 hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the time taken to achieve and total duration of adequate sensory blockade (level of block upto T10) achieved in spinal anesthesia with hyperbaric 0.75% Ropivacaine and hyperbaric 0.5% Bupivacaine in patients undergoing lower limb orthopedic surgeries. <br/ ><br>Timepoint: Before onset and after completion of surgery
- Secondary Outcome Measures
Name Time Method To compare both the study groups for time for first analgesic demand postoperatively. <br/ ><br>Timepoint: After surgery whenever patient complains pain;To compare the motor block achieved with both the study drugs and time taken for full regression of the motor blockTimepoint: Before start and completion of surgery