Status:
COMPLETED
Effects of Perioperative B&O Suppositories on Post-op Pain and Morphine Use After Laparoscopic Prostatectomy
Lead Sponsor:
Benaroya Research Institute
Collaborating Sponsors:
Virginia Mason Hospital/Medical Center
Conditions:
Pain
Eligibility:
MALE
18+ years
Phase:
NA
Brief Summary
This study is evaluating the effect of a Belladonna and Opium suppository administered intraoperatively on post operative pain after laparoscopic radical prostatectomy for prostate cancer. This is a b...
Detailed Description
All patients undergoing LRP at Virginia Mason Medical Center between November 1, 2008 and July 30, 2009 were offered the opportunity to participate in a randomized double blind clinical trial. Operati...
Eligibility Criteria
Inclusion
- Patients scheduled for laparoscopic radical prostatectomy at Virginia Mason, who do not have chronic pain or allergies to opioid analgesics are eligible for this study.
Exclusion
- Women are excluded due to the absence of a prostate.
- Children are excluded due to the absence of prostate cancer in this group.
- Patients meeting any of the following will not be eligible for the study:
- Patients at risk for complications from anticholinergic agents including those with a history of glaucoma, bronchial asthma, convulsive disorder, or high risk for delirium
- History of previous allergies or adverse reactions to belladonna and opium and/or opioid analgesics
- History of chronic pain or chronic use of opioid and nonopioid analgesics
- History of alcohol or opioid dependency/abuse within last three months
Key Trial Info
Start Date :
October 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2009
Estimated Enrollment :
135 Patients enrolled
Trial Details
Trial ID
NCT00863928
Start Date
October 1 2008
End Date
July 1 2009
Last Update
April 23 2019
Active Locations (1)
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1
Virginia Mason Medical Center
Seattle, Washington, United States, 98101