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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00474071 |
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Date of registration:
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14/05/2007 |
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Primary sponsor: |
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Public title:
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Optimum Dose of Remifentanil for Intubation in Small Children
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Scientific title:
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Investigation to Determine the Optimum Dose of Remifentanil for Tracheal Intubation in Children Using the Up/Down Method |
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Date of first enrolment:
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March 2007 |
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Target sample size:
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60 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00474071 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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Countries of recruitment
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Canada
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Contacts
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Name:
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Carolyne Montgomery, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of British Columbia |
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Name:
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Helen Hume-Smith, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of British Columbia |
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Name:
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Mark Ansermino, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of British Columbia |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Presenting for routine endotracheal intubation under anesthesia.
Age minimum:
N/A
Age maximum:
3 Weeks
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Endotracheal Intubation
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Intervention(s)
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Drug: Remifentanil
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Primary Outcome(s)
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Remifentanil intubation dose for ideal intubating conditions
[Time Frame: Unspecified]
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Secondary Outcome(s)
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Cardiovascular effects. Time to return to spontaneous ventilation.
[Time Frame: Unspecified]
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Secondary ID(s)
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H06-03467
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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