Status:
COMPLETED
Comparison of Propofol to Precedex With Propofol for Emergence and Recovery in Patients Having Craniotomy Surgery
Lead Sponsor:
The Cooper Health System
Conditions:
Cranitomy Surgery
Eligibility:
All Genders
Phase:
PHASE3
Brief Summary
Primary Hypothesis: The use of a Precedex infusion, in addition to propofol during surgery, will improve patient management through the anesthesia postoperative recovery period determined by improveme...
Detailed Description
The purpose of this study is to compare the addition of Precedex to a propofol intravenous anesthetic for emergence from anesthesia in patients having craniotomy surgery for brain tumors.
Eligibility Criteria
Inclusion
- ASA status 1, 2, and 3
Exclusion
- ASA status 4 and 5 patients
- Patients with positive pregnancy tests
Key Trial Info
Start Date :
February 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2010
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT00848991
Start Date
February 1 2009
End Date
February 1 2010
Last Update
February 10 2012
Active Locations (1)
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1
Cooper University Hospital
Camden, New Jersey, United States, 08103