Status:
COMPLETED
Co-administration of Propofol and Remifentanil for Lumbar Puncture in Children
Lead Sponsor:
The Hospital for Sick Children
Conditions:
Spinal Puncture
Eligibility:
All Genders
3-12 years
Phase:
PHASE3
Brief Summary
The objective of this study is to compare intraoperative and recovery parameters in patients who receive two different dose combinations of propofol and remifentanil in patients undergoing a lumbar pu...
Detailed Description
Lumbar punctures (LP) are performed in approximately one thousand oncology patients per year at the Hospital for Sick Children. In a previous study, we determined the optimal dose of remifentanil whic...
Eligibility Criteria
Inclusion
- Clinical diagnosis of a hemato-oncological disorder
- Scheduled to undergo a lumbar puncture
- Aged 3-12 years
- Unpremedicated
Exclusion
- children who are known or suspected to be difficult to ventilate by face mask
- children who are deemed medically unfit to receive either of the two study medications
- children who are obese (weight for height \> 95th percentile)
- children who do not have an indwelling intravenous line
Key Trial Info
Start Date :
November 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2007
Estimated Enrollment :
34 Patients enrolled
Trial Details
Trial ID
NCT00405522
Start Date
November 1 2006
End Date
June 1 2007
Last Update
March 8 2019
Active Locations (1)
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1
The Hospital for Sick Children
Toronto, Ontario, Canada, M5G 1X8