Status:
COMPLETED
Stress During Deep Sedation With Propofol With and Without Alfentanil
Lead Sponsor:
Hennepin Healthcare Research Institute
Conditions:
Sedation
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
This is a randomized clinical trial of deep procedural sedation with propofol with and without supplemental alfentanil. Patients will be assessed for total and fractionated serum catecholamines before...
Eligibility Criteria
Inclusion
- patients who will require deep procedural sedation with propofol in the ED
Exclusion
- age \<18
- intoxication
- unable to provide informed consent
- allergy to propofol or alfentanil
- pregnant
- ASA physical status score \> 2
Key Trial Info
Start Date :
October 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2012
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00997113
Start Date
October 1 2009
End Date
December 1 2012
Last Update
September 25 2014
Active Locations (1)
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1
Hennepin County Medical Center
Minneapolis, Minnesota, United States, 55415