CompletedPhase 4ketamine

Ketamine and Propofol for Upper Endoscopy

Sponsored by The Hospital for Sick Children

NCT ID
NCT02295553
Target Enrollment
56 participants
Start Date
2013-07
Est. Completion
2016-12

About This Study

The purpose of this study is to examine the dose-response relationship of ketamine in combination with propofol.

Conditions Studied

Anesthesia

Interventions

  • Ketamine
  • Propofol

Eligibility

Age:3 Years - 13 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Age 3-13 years
* Receiving general anesthesia for upper endoscopy

Exclusion Criteria:

* Known or possible difficult airway
* BMI \> 35
* Weight \< 10 kg
* Sedative premedication required
* Known contraindication to ketamine or propofol

Study Locations (1)

The Hospital for Sick Children
Toronto, Ontario, Canada

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source