Clinical Trials Directory

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

TypeNameDescription
PROCEDUREControlDeflated blood pressure cuff placed on upper arm for 30min
PROCEDURERemote ischemic preconditioningBlood 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.