MedPath

To compare the effect of two methods of propofol drug delivery during induction of general anesthesia

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/07/070229
Lead Sponsor
ewlyna Eireeka Ivan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

ASA I-III scheduled under GA with Propofol as the agent of intravenous induction

Exclusion Criteria

1. Patient refusal to participate

2. Patients with known allergy to egg

3. Patients scheduled for emergency surgeries, patients with severe valvular heart disease

Study & Design

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