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A clinical trial to study the effect of different doses of phenylephrine hydrochloride for treatment of fall in blood pressure during spinal anaesthesia in patients undergoing planned caesarean sectio

Phase 4
Completed
Conditions
Health Condition 1: null- Spinal anaesthesia induced hypotension
Registration Number
CTRI/2011/12/002294
Lead Sponsor
niversity College of Medical Sciences and Guru Teg Bahadur Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
120
Inclusion Criteria

ASA I or II females with term, uncomplicated, singleton pregnancy undergoing elective LSCS under spinal anaesthesia

Patients who develop hypotension after subarachnoid block will be included

Hypotension after spinal anaesthesia will be defined as a fall of > 20% from the baseline or an absolute value of less than 100 mm Hg systolic blood pressure

Exclusion Criteria

Maternal complications e.g. diabetes, pregnancy induced hypertension, cardiovascular disease, cerebrovascular disease

Placental complications viz., placenta praevia or abruptio placentae

Cord complications viz., nuchal cord or cord prolapse

Foetal malformations

Patients with absolute or relative contra-indications for spinal anaesthesia e.g. infection in lumbar area, coagulation abnormalities, autonomic neuropathy, spinal deformities, other neurological diseases, hypovolemia due to any cause

Maternal baseline SBP less than 100 mmHg

Patients with baby birth weight less than 2.5 kg or greater than 4.5 kg

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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