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Phenylephrine Infusion Versus Bolus Regimens During Caesarean Delivery Under Spinal Anaesthesia:an observational study to Assess Hemodynamic Changes.

Not Applicable
Registration Number
CTRI/2020/04/024807
Lead Sponsor
HARSHNI K
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients undergoing elective caeserean section

ASA 2

AGE 18 YEARS and above

Weight 50 to 100kgs

Height 150 to 180cms

Singleton pregnancy

Exclusion Criteria

Patient refusal

Allergy to phenylephrine

Hypertension,cardiovascular,cerebrovascualr,pulmonary or endocrine diseases

Fetal abnormalities

Multiple pregnancy

Contraindications to spinal anesthesia

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Heart rate <br/ ><br>Blood pressureTimepoint: Heart rate less than 60 <br/ ><br>Blood pressure than 20% of the baseline
Secondary Outcome Measures
NameTimeMethod
Side effects <br/ ><br>APGAR score of newbornTimepoint: Side effects like hypertension <br/ ><br>APGAR score of newborn less than 7
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