Prevention of spinal hypotension using phenylephrine infusio
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indicationHealth Condition 2: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/10/046552
- Lead Sponsor
- S Nijalingappa medical college and HSK hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASAIâ??II patients.
2.Parturients aged between18â??40years.
3.Parturients undergoing elective caesarean delivery.
Exclusion Criteria
1.Refusal at enrolment.
2.Parturients with pregnancy induced hypertension
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3.Parturients with risk of excessive bleeding. (Placenta previa, prolonged labor
multiple gestation, abruptio placenta,
4.Parturients with cerebro vascular diseases, gestational diabetes, anemia,
5.Parturients with known allergy to phenylephrine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the effect of prophylactic phenylephrine infusion in <br/ ><br>prevention of hypotension post spinal anaesthesia. <br/ ><br>Timepoint: 60 min <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare the incidence of nausea, vomiting with control groupTimepoint: 60 min