COMPARISON OF LATERAL AND SITTING POSITIONS DURING SPINAL ANAESTHESIA FOR CESAREAN SECTIO
Not Applicable
- Conditions
- Health Condition 1: null- pregnant Women for cesarean section
- Registration Number
- CTRI/2014/06/004675
- 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
- 100
Inclusion Criteria
•Singleton pregnancy
•Age 18-45 years
•Woman for cesarean section as per obstetrical indication
•Period of gestation between 36 to 41 weeks
Exclusion Criteria
•twin pregnancy
•severe pre-eclampsia/ HELLP syndrome
•Co-agulopathy
•Abruptio placentae
•Intra-uterine fetal death/Malformed fetus
•Uncontrolled diabetes mellitus
•Chorio-amniotis
•Known case of thrombophilia
•Known case of chronic Renal or liver disease
•previous classical caesarean section/ hysterotomy
•previous uterine surgery other than caesarean section (myomectomy, hysterotomy, polypectomy, lysis of uterine synechia, or hysteroscopic metroplasty)
•women who do not achieve sensory level T6 or Bromage score 3, 15 minutes after intrathecal injection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is comparison of fall in blood pressure in two groups.Timepoint: from intra-thecal injection to two hours after completion of surgery
- Secondary Outcome Measures
Name Time Method â?¢Lowest recorded systolic BP <br/ ><br>â?¢Lowest recorded Mean Arterial Pressure (MAP) <br/ ><br>â?¢Onset of hypotension (20% fall in systolic BP or 90 mm Hg) <br/ ><br>â?¢Use of phenylephrine <br/ ><br>â?¢Upper sensory level <br/ ><br>â?¢Time to achieve sensory level T6 <br/ ><br>Timepoint: from intra-thecal injection to two hours after completion of surgery