MedPath

A comparative study between two drugs used as an additive to spinal anaesthesia drug in surgeries for removal of uterus

Not Applicable
Completed
Conditions
Health Condition 1: null- Fibroid uterus , Dysfunctional uterine bleeding
Registration Number
CTRI/2018/01/011615
Lead Sponsor
Dr Vinod C
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Patients belonging to ASA 1 and 2

Exclusion Criteria

allergy to the study drug

patients with heart blocks / dysrrhythmias

Failure of spinal anaesthesia

Study & Design

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