Adding additive to spinal drug to see for pain relief after surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063780
- Lead Sponsor
- Ananya Krishna T
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA1 and 2 patients undergoing elective lower abdominal surgery under subarachnoid block.
Exclusion Criteria
All ASA 3 and 4
Patients with spinal deformity
Pregnant patients
Patients with height less than 140cm
Patients with known drug allergy, preexisting cardiovascular, respiratory and neurological disorders
Patients with local skin infections, impaired liver or renal function tests, coagulation disorders
Patients with BMI more than 30kg/m2
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to assess onset and duration of sensory blockade, maximum sensory blockade and the time taken for it, time taken for 2 segment regression, onset and duration of motor blockade, total duration of postoperative analgesia.Timepoint: 1,2,3,4,5,10,15,20,25,30,35,40,45,50,55,60,65,70,75,80,85,90 minutes and till 3 hours postoperative period
- Secondary Outcome Measures
Name Time Method changes in heart rate, SBP,DBP,MAPTimepoint: 1, 1 1/2,2,21/2,3 hours