drugset / Trial / NCT01770236

Pain Control After Minimally Invasive Coronary Artery Bypass Grafting

NCT01770236 ↗

Phase 4 Terminated 41 enrolled Gundersen Lutheran Medical Foundation
RandomizedParallel-groupOpen-labelSupportive care

Summary

The purpose of this study is to compare postoperative pain control after minimally invasive coronary artery bypass grafting for patients who receive an intercostal block (an anesthetic medicine injected in an area under the ribs) in the operating room and IV acetaminophen (Tylenol) to those who receive an intercostal block and On-Q pain pump catheter (a balloon pump attached to 2 small tubes near your procedure site that automatically delivers pain medicine).

Timeline

Start
2013-01
Primary completion
2015-11
Completion
2015-11

Outcome

Outcome not reported

Stopped: “Study medication no longer available at institution”

Drugs

EvaluationDrugModalityDoseRoute
Subject Acetaminophen Small molecule 1000 mg Intravenous

Indications

No indication recorded.