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
| Type | Name | Description |
|---|---|---|
| DRUG | IV acetaminophen | Patients 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.