Status:
WITHDRAWN
Clinical Study of Depodur Efficacy in Decreasing Post Operative Pain After Off Pump Coronary Artery Bypass Grafting (OP-CABG)
Lead Sponsor:
Drexel University College of Medicine
Conditions:
Pain, Postoperative
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The purpose of this study is to determine whether epidural Depodur alleviates the pain of OP-CABG surgery. This includes pain associated with sternotomy, retraction, dissection and other tissue insult...
Detailed Description
The purpose of this study is to determine whether epidural Depodur alleviates the pain of OP-CABG surgery. This includes pain associated with sternotomy, retraction, dissection and other tissue insult...
Eligibility Criteria
Inclusion
- Male or Female, 18-99 years old
- All patients who will have surgery for OP-CABG
Exclusion
- Pregnant females
- Patients with allergy to morphine
- Patients nursing an infant
- Patients with migraine headaches
- Patients taking Coumadin within 7 days or demonstrating INR \> 13
- Patients taking Heparin unless documented normal partial thromboplastin time
- Patients taking Clopidogrel in previous 7 days
- Patients taking Ticlopidine in previous 14 days
- Patients taking Aspirin in previous 48 hours
- Patients receiving low molecular weight heparin therapy within 24 hours previous
- Patients with Narcolepsy and/or sleep apnea
- Patients on chronic opioid therapy
- Patients participating in another study
Key Trial Info
Start Date :
April 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2008
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00456638
Start Date
April 1 2008
End Date
April 1 2008
Last Update
August 15 2014
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