Clinical Trials Directory

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

TypeNameDescription
PROCEDURERemote ischemic conditioningPatients 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.
PROCEDUREShamPatients 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.

Remote Ischemic Conditioning and Atrial Fibrillation After Coronary Artery Bypass Grafting (CABG) (NCT01107184) · Clinical Trials Directory