Comparison of two drugs for premedication in children planned for MRI
Phase 4
- Conditions
- Health Condition 1: G00-G99- Diseases of the nervous system
- Registration Number
- CTRI/2024/05/066613
- Lead Sponsor
- Department of Anesthesia and Pain Medicine Pt JNM Medical College Raipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA GRADE I AND II
BODY WT 10-20 KG
SCHEDULED FOR MRI UNDER SEDATIO
Exclusion Criteria
1.Not nil by mouth
2.Parents refusal
3.Duration of scan more than 60-90 mins
4 Congenital heart disease, upper respiratory tract infection,
5.Pts. on Antipsychotics, Anticonvulsants, any sedative drugs.
6. Pts with altered sensorium
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of sedation as assessed by OAA/S scale <br/ ><br>(Observer Assessment of Alertness/Sedation Score)Timepoint: The time of dosage will be noted, and the observer will record SpO2, HR and the sedation level at 5-min intervals for 30min following drug administration. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Onset of sedation <br/ ><br>2. Ease of Parental Separation <br/ ><br>3.Changes in Hemodynamic parameters <br/ ><br>4.Total dose of requirement of supplemental Fentanyl. <br/ ><br>Timepoint: The time of dosage will be noted, and the observer will record SpO2, HR at 5-min intervals for 30min following drug administration. <br/ ><br>