Spinal anaesthesia with two different drugs as adjuvants in cesarean sectio
Not Applicable
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/05/067057
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for elective or emergency caesarean section receiving spinal anaesthesia Patients in the age group of 18-40 years
Patients belonging to ASA grade I, II or III
Patients giving written informed consent
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset and duration of sensory & motor blockade <br/ ><br>Duration of post operative analgesia and 24 hours analgesic requirementTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Sensory assessment: pin prick method <br/ ><br>Modified Bromage scale <br/ ><br>Apgar score <br/ ><br>Visual analogue scale score for pain <br/ ><br>Ramsay sedation scoreTimepoint: Till 24 hrs after spinal anaesthesia