Trials / Completed
CompletedNCT01390129
Remote Ischemic Preconditioning in Aortic Valve Surgery
Remote Ischemic Preconditioning in Aortic Valve Surgery (RIP-Valve)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- University Hospital, Angers · Other Government
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
RIP-VALVE is a randomized, single blinded study that will test the hypothesis that remote ischemic preconditioning initiated before surgery reduces post-operative myocardial damage in aortic valve surgery. Infarct size will be determined by 72 hours area under curve of troponin-I.
Detailed description
The hypothesis tested in this research proposal is that remote ischemic preconditioning initiated immediately before aortic valve surgery reduces myocardial damage related to surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Control | Deflated blood pressure cuff placed on upper arm for 30min |
| PROCEDURE | Remote ischemic preconditioning | Blood pressure cuff placed on upper arm and inflated to 200 mmHg for 5 min and then deflated for 5 min. This cycle is initiated before aortic clamping and repeated 3 times in total |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2011-07-08
- Last updated
- 2012-10-24
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT01390129. Inclusion in this directory is not an endorsement.