Clinical Trials Directory

Trials / Terminated

TerminatedNCT01770236

Pain Control After Minimally Invasive Coronary Artery Bypass Grafting

Optimal Method of Pain Control After Minimally Invasive Coronary Artery Bypass Grafting

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Gundersen Lutheran Medical Foundation · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGIV acetaminophenPatients randomized to the IV acetaminophen group will receive IV acetaminophen (1000 mg every 6 hours for adults and weight-based for any patient under 50 kg)instead of an On-Q pain pump catheter.

Timeline

Start date
2013-01-01
Primary completion
2015-11-01
Completion
2015-11-01
First posted
2013-01-17
Last updated
2016-12-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01770236. Inclusion in this directory is not an endorsement.