Vasopressor of choice for spinal hypotension in elective Cesareansectio
Not Applicable
Completed
- Conditions
- Health Condition 1: O746- Other complications of spinal andepidural anesthesia during labor and deliveryHealth Condition 2: null- PREGNANT PATIENTS AT TERM GESTATIO
- Registration Number
- CTRI/2018/07/014976
- Lead Sponsor
- Kovai Medical Center and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 72
Inclusion Criteria
1. ASA I and II,
2. Singleton gestation >36 weeks,
3. Scheduled elective cesarean delivery
under spinal anesthesia,
4. Fasting >6 h
Exclusion Criteria
1. Pregnancy-related hypertensive disease,
2. Multiple gestation,
3. Gestational diabetes requiring insulin,
4. Documented history of postoperative nausea
and vomiting,
5. Body mass index (BMI) >40 kg/m2,
6. Emergency caesarean section for maternal
and/or fetal distress,
7. ASA III and IV patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To maintain maternal systolic and diastolic blood pressure in term parturients during spinal anaesthesia.Timepoint: The study infusion medication is started at the same time cerebrospinal fluid was obtained, immediately before injection of spinal medications. Blood pressure measured every minute from the start of study medication infusion till the baby delivery.
- Secondary Outcome Measures
Name Time Method ausea and vomitingTimepoint: intraoperative time;Apgar scoreTimepoint: at 1st and 5th minute of life;fetal heart rateTimepoint: at 5th minute of life;Maternal heart rateTimepoint: Every minute, from the time of start of infusion medication till the baby delivery.;perfusion indexTimepoint: every minute,from start of study medication infusion till the time of baby delivery;rescue boluses usedTimepoint: When blood pressure and heart rate falls below 20 percent of baseline values.;umblical cord blood analysisTimepoint: cord blood sample will be withdrawn just before delayed cord clamping.