MedPath

To assess the time of onset and efficacy of sensory and motor blockade and post operative pain when two different Adjuvants are added to hyperbaric levobupivacaine for spinal anaesthesia to pregnant patients undergoing caesarean sectio

Phase 4
Conditions
Health Condition 1: O- Medical and SurgicalHealth Condition 2: Z331- Pregnant state, incidental
Registration Number
CTRI/2024/05/068208
Lead Sponsor
Pithani Vamsee Priya
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Pregnant females posted for LSCS under spinal anaesthesia

ASA-II

Exclusion Criteria

Patients not willing to be part of study

Contraindications of subarachnoid block

Allergy to local anaesthesia

Twin pregnancies

Polyhydramnios

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath