comparing the 2 modes of administering phenylepjerine(in the muscle vs intravenous) for preventing fall in blood pressure in pregnant females getting caesarean section done under spinal anaesthesia
Not Applicable
- Conditions
- Health Condition 1: 1- ObstetricsHealth Condition 2: O748- Other complications of anesthesiaduring labor and delivery
- Registration Number
- CTRI/2021/02/031200
- Lead Sponsor
- Department of anaesthesia PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Caesarean Section
2. Singleton pregnancy at term
3. 18 â?? 35 years old
4. Height 150 â?? 180 cm
Exclusion Criteria
1. BMI <18.9 and >34.9
2. Refusal of Consent
3. Multiple Pregnancy
4. Pregnancy induced hypertension/ eclampsia/ peripartum bleeding/women in labour
5. Known cardiac disease or chronic hypertension.
6. Foetal distress or complications
7. Contraindication for spinal anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the umbilical cord blood base excess(BE) between the two groups. <br/ ><br>Timepoint: at the time of baby delivery, immediately after cord clamping <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. To compare the incidence of maternal hypotension in the two groups. <br/ ><br>2. Incidence of bradycardia and reactive hypertension. <br/ ><br>3. Intraoperative nausea vomiting. <br/ ><br>4. Umbilical cord blood parameters apart from BE. i.e. pH, lactate levels.Timepoint: The first three secondary outcomes will be measured every 5 min(5,10,15,20,25,30,35,40,45,50,55,60 min) till the end of surgery. <br/ ><br>4th secondary outcome is at the delivery of baby, immediately after cord claping