Comparison of two drugs in spinal anaesthesia for lower abdominal and lower limb surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/11/047419
- Lead Sponsor
- ROHILKHAND MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of anaesthesiologist (ASA) grade I and II
Patients posted for lower abdominal and lower limb surgery under different surgical specialty
Exclusion Criteria
Any Neuropathy
Any known allergy to Local anaesthetic
Patients with contraindications for spinal anaesthesia such as deranged coagulation profile, raised ICP, local infection at site of needle insertion.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Hemodynamic changes <br/ ><br>2. Onset of sensory and motor blockade <br/ ><br>3. Sensory and motor blockade characteristics <br/ ><br>Timepoint: The patient will be evaluated for sensory and motor block, for every 2 minutes for first 20 minutes, every 3 minutes for next 30 minutes, every 10 minutes for 60 minutes, and finally every 15 minutes until the sensory block has regressed to S1 dermatome.
- Secondary Outcome Measures
Name Time Method 1. Time for first rescue analgesia <br/ ><br>2. Any complications <br/ ><br>Timepoint: patientâ??s pulse, Systolic Blood pressure, Diastolic Blood pressure, Mean Arterial Pressure, heart rate will be recorded every 3 minutes for 30 minutes and then every 5 mins for next 30mins and then 15mins until completion of the surgery.