The study to compare two different dose of norepinephrine based on weight of the patient for preventing fall in blood pressure after spinal anaesthesia in patients undergoing cesarean sectio
Phase 2
Completed
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/02/062991
- Lead Sponsor
- SK Saif ali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 170
Inclusion Criteria
1)full term women undergoing elective cesarean section
2) ASA class II
3)age between 18-35 years
Exclusion Criteria
1) patients refusal
2)hypertensive disorders
3)cardiac diseases
4)allergy to local anaesthetics
5)obstretic complications (antepartum hemorrhage,placenta privea,placental abruption)
6)coagulopathy,sepsis,hepatic or renal failure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)Doses of rescue bolus of phenylephrine 20 mcg <br/ ><br>2)access incidence of hypotension in both groupsTimepoint: Incidence of hypotension is assessed immediately after spinal anaesthesia measurement of blood pressure every 1 minute after spinal till the delivery of baby and the amount of PHENYLEPHERINE boluses used during the intraoperative period.
- Secondary Outcome Measures
Name Time Method 1)intraoperative blood pressure(systolic and diastolic h <br/ ><br>Pressure) <br/ ><br>2)mean arterial pressure <br/ ><br>3)post operative shiveringTimepoint: 1)intraoperative blood pressure at baseline and 1minute after spinal anaesthesia till end of the procedure <br/ ><br>2)post operative shivering accessed after giving spinal anaesthesia and in the post anaesthetic care unit <br/ ><br>3)mean arterial pressure at baseline and 1 minute after giving spinal anaesthesia till the end of procedure