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minimum duration required between premedicating agents and inducing agents to decrease the dose required for inducing agent and to maintain better vital parameters

Phase 4
Conditions
Health Condition 1: null- Posted for surgery under general anaesthesia
Registration Number
CTRI/2017/08/009313
Lead Sponsor
Department of Anaesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients belonging to American Society of Anesthesiologists physical status I & II

2.Patients undergoing neuro-surgery

3.Age group between 15 and 50 years

4.Haemodynamically stable

Exclusion Criteria

1.History of hypertension, diabetes or other systemic illness

2.History of drug or alcohol abuse

3.History of neurological disease

4.History of chronic use of opioid, antipsychotic, antidepressant, anxiolytic drug.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in dose of propofolTimepoint: 10 minutes
Secondary Outcome Measures
NameTimeMethod
Maintainance of hemodynamic parametersTimepoint: 10 minutes
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