Pain Control After Minimally Invasive Coronary Artery Bypass Grafting

Status Terminated

Clinical Trial 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).

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Drug-Related Side Effects and Adverse Reactions
Medication Side Effects
Narcotic Requirement
Pain, Postoperative
Postoperative Pain

Clinical Trial Details

NCT number	NCT01770236
Study type	Interventional
Source	Gundersen Lutheran Medical Foundation
Contact
Status	Terminated
Phase	Phase 4
Start date	January 2013
Completion date	November 2015

View Details

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