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comparing the effectiveness of different doses of norepinephrine immediately after giving spinal anaesthesia to prevent fall in blood pressure during caesarean section.

Not Applicable
Completed
Conditions
Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
Registration Number
CTRI/2020/04/024801
Lead Sponsor
Kasturba medical college
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
80
Inclusion Criteria

1.Pregnant females undergoing elective caesarean section under spinal anaesthesia.

2.Full term pregnancy.

3.Singleton pregnancy.

4.BP range 90-140 mmHg

5.ASA physical status II

6.Age 18 years and older.

7.Weight between 50 and 100 kg.

8.Height between 150 and 170 cm.

Exclusion Criteria

1. Patient refusal.

2. Hypertension, cardiovascular or cerebrovascular disease.

3. Fetal abnormalities.

4. Diabetes (excluding gestational diabetes).

5. Contraindications to spinal anaesthesia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Success of prophylactic iv bolus of norepinephrine to maintain SBP at or above 80% of baselineTimepoint: from induction to delivery of foetus
Secondary Outcome Measures
NameTimeMethod
<br/ ><br>1.Hypertension <br/ ><br>2.Bradycardia <br/ ><br>3.nausea and vomiting <br/ ><br>4. APGAR score <br/ ><br> <br/ ><br>4.Nausea <br/ ><br>5.Vomiting <br/ ><br>6.Apgar score <br/ ><br>Timepoint: From induction to delivery of baby
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