To compare norepinephrine and phenylephrine infusion to prevent spinal anesthesia induced hypotensio
Not Applicable
Completed
- Conditions
- Health Condition 1: O295- Other complications of spinal andepidural anesthesia during pregnancy
- Registration Number
- CTRI/2019/12/022505
- Lead Sponsor
- Vijayanagar Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 156
Inclusion Criteria
1.American Society of Anesthesiologists physical status 2
2.Singleton term pregnancy
Exclusion Criteria
1.Age less than 18 years
2.Height less than 150cm or more than 180cm
3.Weight less than 50kg or more than 100kg
4.Contraindication to spinal anaesthesia
5.Allergy to drugs used in the study
6.Eclampsia,preeclampsia,placenta previa,diabetes mellitus,hypertension,cardiovascular disease or refusal to be in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of hypotensionTimepoint: Study parameters are observed and recorded just before spinal anaesthesia and thereafter every minute after spinal anaesthesia until 10 min after baby extraction
- Secondary Outcome Measures
Name Time Method Incidence of hypertension, APGAR score of the baby, bradycardia, tachycardia, nausea and vomittingTimepoint: Study parameters are observed and recorded just before spinal anaesthesia and thereafter every minute after spinal anaesthesia until 10 min after baby extraction