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Clinical Trials/CTRI/2013/09/004031
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Department of Anaesthesia ESI PGIMSR

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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