Comparision of Norepinephrine and Phenylephrine for maintenance of blood pressure during spinal anaesthesia in caesarean delievery.
Phase 4
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2018/10/016008
- Lead Sponsor
- Government medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Singleton full term pregnancy.
ASA I/II
Scheduled for elective LSCS under spinal anaesthesia
Exclusion Criteria
-Contraindication to spinal anaesthesia,
-patient refusal,hypertension
-allergic to study drug
-Arrythmia,morbid obesity,
-known fetal abnormality
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method monitoring of vital parameters such as heart rate, blood pressure, spo2, ECG, non invasive cardiac outputTimepoint: monitoring vital parametrs at 1,3,5,10,15,20,30,45,90,120,150 minutes.
- Secondary Outcome Measures
Name Time Method -Apgar score , to see the effect on fetus. <br/ ><br>-Total no of doses of study drug required. <br/ ><br>-perioperative complications such as bradycardia,hypertension, <br/ ><br>arrythmias,nausea vomiting, respiratory depression.Timepoint: Check for apgar score at 1, 5 ,10 min.