Status:
COMPLETED
Anesthesia and Postoperative Pain
Lead Sponsor:
Columbia University
Conditions:
Postoperative Pain
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare post-operative pain after anesthesia with either isoflurane or propofol. Each group will be further randomized to receive intranasal nicotine or placebo in orde...
Detailed Description
A. Study Proposal and Rational The purpose of this study is to determine whether intranasal nicotine can decrease the negative side effects of the general anesthetic isoflurane. Isoflurane and other ...
Eligibility Criteria
Inclusion
- greater than or equal to 18 years of age
- female sex
- present to New York Presbyterian Hospital for open pelvic surgery
Exclusion
- smoking
- uncontrolled hypertension
- myocardial disease
- history of stroke
Key Trial Info
Start Date :
July 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2006
Estimated Enrollment :
23 Patients enrolled
Trial Details
Trial ID
NCT00232817
Start Date
July 1 2003
End Date
March 1 2006
Last Update
July 12 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
New York Presbyterian Hospital
New York, New York, United States, 10032