Trials / Terminated
TerminatedNCT01107184
Remote Ischemic Conditioning and Atrial Fibrillation After Coronary Artery Bypass Grafting (CABG)
A Clinical Study on the Effect of Remote Ischemic Conditioning on Atrial Fibrillation and Outcome After Coronary Artery Bypass Grafting
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 191 (actual)
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Recent studies indicate that remote ischemic conditioning can protect the heart and other organs during cardiac surgery. The investigators aim to investigate whether such a stimulus can reduce the incidence of atrial fibrillation or other complications following coronary artery bypass surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Remote ischemic conditioning | Patients will have a automated inflator cuff placed on the upper arm during surgery. The cuff will be used to induce fore arm ischemia by inflation to 200 mmHg for 3 x 5 minutes, interspersed with 5 minutes of no-inflation and thus reperfusion. |
| PROCEDURE | Sham | Patients will have a automated inflator cuff placed on the upper arm during surgery which will not be inflated. |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2016-02-01
- Completion
- 2016-02-01
- First posted
- 2010-04-20
- Last updated
- 2018-02-01
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT01107184. Inclusion in this directory is not an endorsement.