Clinical trial to study the effect of oral carbohydrate solution given before surgery in women undergoing elective Caesarean delivery under spinal anesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2021/11/038230
- Lead Sponsor
- Directorate of Medical Education Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Full-term pregnancy (>=37 weeks estimated gestational age)
Singleton gestation
Exclusion Criteria
1) Pre-gestational or gestational diabetes
2) Incomplete gestational diabetes screening
3) History of steroid administration within 7 days prior to planned delivery
4) History of magnesium sulphate administration because of hypertensive disorder of pregnancy
5) Current opioid use
6)Foetus with congenital anomalies or growth
restriction
7) American Society of Anaesthesiology physical class III or greater
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preoperative well being <br/ ><br>Visual analogue scale (VAS) for hunger, thirst, anxiety, fatigue, and nausea administered on the morning of surgery. <br/ ><br> <br/ ><br>Timepoint: In the preopeartive room prior to surgery. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Incidence of post-spinal hypotension â?? systolic blood pressure of less than 100mmHg or decrease in more than 20% of baseline. <br/ ><br> <br/ ><br>Timepoint: Intraoperative after spinal anesthesia. <br/ ><br>;Blood sugar level of patient immediate before surgery and on Day 1 post-operative.Timepoint: Prior to surgery and fasting blood sugar in the morning on postoperative day 1;Cord blood sugar estimationTimepoint: Immediately after delivery;Incidence of intra operative nausea & vomitingTimepoint: Intraoperative;Post-operative satisfaction as measured by Quality of Recovery from Anaesthesia questionnaire(QoR-40)Timepoint: Post operatively 24 hours after suregry.;Total Phenylephrine useTimepoint: Intraoperative