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A Clinical study to find the effect of melatonin in reducing stress to intubation in patients undergoing surgeries.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/05/066842
Lead Sponsor
BGS Global Institute of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Patients willing to give written informed consent.

2. ASA physical status I,II.

3. Patients posted for elective surgery under general anaesthesia with endotracheal intubation.

Exclusion Criteria

1. Patients with anticipated difficult Intubation.

2. Patients with ASA physical status III and above.

3. Patients allergic to study drug.

4. Patients with steroids and antipsychotics.

5. Patients with history of active seizure disorders or active neurological disorders.

6. Patients with history of chronic alcoholism.

7. Patients with greater than 30kg per meter square.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study the effect of preoperative sublingual melatonin 6mg on the pressor response by monitoring the hemodynamic changes to laryngoscopy and intubation.Timepoint: 1 hour before induction, immideately after intubation - 1min, 3min, 5min ,10 min and 15 minutes after intubation.
Secondary Outcome Measures
NameTimeMethod
To study the adverse effects of sublingual melatonin like dizziness and nausea.Timepoint: 2 hours
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