A trial to compare two different drugs for spinal anaesthesia to prolong duration of analgesia during cesarean sectio
Not Applicable
- Conditions
- Health Condition 1: null- women for cesarean section
- Registration Number
- CTRI/2014/06/004680
- Lead Sponsor
- Govt of Himachal Pradesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
•Singleton pregnancy
•Woman for cesarean section as per obstetrical indication
•Period of gestation between 36 to 41 weeks
Exclusion Criteria
•American society of Anesthesiologist grade >II
•Renal or hepatic impairment
•Thrombocytopenia
•HELLP syndrome
•Patient on magnesium therapy
•Acute fetal distress
•Contraindications to spinal anesthesia
•Morbid Obesity (BMI > 38 kg/m 2)
•Sensitivity to local anesthetic drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome will be the duration of spinal anesthesia in the study groups.Timepoint: six months
- Secondary Outcome Measures
Name Time Method â?¢Time taken for onset of sensory block <br/ ><br>â?¢Time taken for onset of motor block <br/ ><br>â?¢Time taken to achieve maximal sensory block <br/ ><br>â?¢Duration of sensory block <br/ ><br>â?¢Duration of motor block <br/ ><br>â?¢Need and amount of rescue analgesia <br/ ><br>Timepoint: â?¢Time taken for onset of sensory block <br/ ><br>â?¢Time taken for onset of motor block <br/ ><br>â?¢Time taken to achieve maximal sensory block <br/ ><br>â?¢Duration of sensory block <br/ ><br>â?¢Duration of motor block <br/ ><br>â?¢Need and amount of rescue analgesia <br/ ><br>