se of epidural colloid for comparison of low doses of intrathecally administered bupivacaine
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Booked to deliver by caesarean section
- Registration Number
- CTRI/2011/10/002037
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 204
Inclusion Criteria
ASA Physical Status I or II,
height 145-165 cm,
body mass index of 25+/-10%,
> 37 weeks of gestation,
single nun-complicated pregnancy
Exclusion Criteria
weight more than 100 kg,
pregnancy-induced hypertension,
end-organ disease,
in active labour,
emergency caesarean section
any contraindication to regional anaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of effective dosesTimepoint: During intraoperative period
- Secondary Outcome Measures
Name Time Method Adequecy of muscle relaxationTimepoint: By operating surgeon during intraoperative period;APGAR scoreTimepoint: Of neonate at 1 and 5 min after birth;ComplicationsTimepoint: During intraoperative period;Degree of lower limb motor blockTimepoint: At 5 min intervals for the first 20 min after giving combined spinal epidural anaesthesia and at 10 min intervals thereafter.;Need of epidural top-upsTimepoint: During intraoperative period;Time to modified bromage score 6Timepoint: Post operative period;Time to sensory regression to T10 levelTimepoint: Post operative period;Upper level of dermatomal sensory blockTimepoint: At 5 min intervals for the first 20 min after giving combined spinal epidural anaesthesia and at 10 min intervals thereafter.