Status:
COMPLETED
A Prospective, Randomized, Blinded Study of BIS Analysis in ICU Patients Requiring Neuromuscular Blocking Agents
Lead Sponsor:
University of Utah
Conditions:
ICU Patients
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This is a prospective, randomized, blinded study in which patients will be enrolled into either treated(BIS group) or untreated (non-BIS) group employing bispectral analysis to measure the level of se...
Detailed Description
This is a prospective, randomized and blinded study being done in order to help evaluate the level of consciousness with bispectral analysis (BIS) in ICU patients who are pharmacologically paralyzed w...
Eligibility Criteria
Inclusion
- Consented ICU patient, receiving neuromuscular blocking agents.
Exclusion
- Unable to be consented
Key Trial Info
Start Date :
February 1 2000
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2007
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT00714974
Start Date
February 1 2000
End Date
October 1 2007
Last Update
July 14 2008
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