CTRI/2013/09/004031
Completed
Phase 4
Evaluation of varying doses of propofol infusion after low dose ketamine for ambulatory paediatric magnetic resonance imaging.
Department of Anaesthesia ESI PGIMSR0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Department of Anaesthesia ESI PGIMSR
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ASA status 1 or2 patients in age gp 6 mths to 10 yrs for elective MRI
Exclusion Criteria
- •ASA status 3 or above, severe cardiovascular or pulmonary pathology;
- •documented allergy or intolerance to propofol ; anatomical anomaly of airway; tonsillar hypertrophy grade 3 or above; MRI for acute trauma.
Outcomes
Primary Outcomes
Not specified
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