MedPath

A Clinical trial to study the effects of three drugs- Ondansetron, Lidocaine and Dexamethasone in relieving pain caused by injection of Propofol during induction of sleep during general anaesthesia.

Phase 4
Conditions
Health Condition 1: null- COMING FOR ELECTIVE SURGERY UNDER GENERAL ANESTHESIA WITH NO HYPERTENSION/DIABETES MELLITES
Registration Number
CTRI/2017/11/010628
Lead Sponsor
Department of Anesthesiology St johns medical college hospital Bangalore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients in the age group 18-59 yrs

2.American society of anaesthesiology (ASA) physical status I and II.

3.All general surgical procedures .

Exclusion Criteria

1. Patients with allergy to propofol, lignocaine.

2. Patients with anticipated difficult airway

3. Patients with cardiac conduction defects, congenital heart diseases

4. Haemodynamic instability

5. Patients with chronic pain syndromes.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of pre-treatment with lidocaine, ondansetron or dexamethasone in reducing the pain of propofol injection in adult patients scheduled for surgical procedures under general anaesthesia. <br/ ><br> <br/ ><br>Timepoint: assessment of pain scoring 15 seconds after administering propofol <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To assess any reaction to the drug at injection site.Timepoint: at the end of general surgical procedure approximately 60-90 minutes.
© Copyright 2025. All Rights Reserved by MedPath