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Clinical trial to study the comparison of two doses of nebulised dexmedetomidine in paediatric patients

Phase 4
Recruiting
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/04/042068
Lead Sponsor
gopal krishan jalwal
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patient of either sex in the age group of 3 to 8 years belong to ASA 1 or II

2. Patient scheduled for elective infraumblical and lower limb surgeries under general anaesthesia with endotracheal intubation

Exclusion Criteria

1. Patient with history of cardiac disease, asthma, seizure disorders, mental retardation, developmental delay, prematurity and allergy will be excluded from the study

2. Surgeries performed under general anaesthesia using supraglottic airway device.

3. Emergency surgeries

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of two doses of nebulised dexmedetomidine as premedication in paediatric patients for parental separation anxietyTimepoint: patient separation anxiety scale will be assessed while shifting the patient to OT <br/ ><br>time point : 24 weeks
Secondary Outcome Measures
NameTimeMethod
1) To compare Mask acceptance score, sedation score, haemodynamic variables, emergence scoresTimepoint: 6 months
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