Clinical Trials Directory

Trials / Completed

CompletedNCT03866395

Effects of Ivabradine on Residual Myocardial Ischemia After PCI

Effects of Ivabradine on Residual Myocardial Ischemia After PCI Evaluated by Stress Echocardiography

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
28 (actual)
Sponsor
Azienda Policlinico Umberto I · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a randomized pharmacological study evaluating the effects of ivabradine in patients with residual angina after PCI. The role of ivabradine in patients with angina, without systolic dysfunction, is not yet clear. The investigators performed in all patients an echostress to evaluate the effects of therapy with ivabradine after 30 days in terms of exercise tolerance and diastolic function.

Detailed description

BACKGROUND. Residual angina after PCI is a frequently-occurring disease. Ivabradine improves symptoms but its role in patients without left-ventricular systolic dysfunction is still unclear. The aim was to quantify the effects of ivabradine in terms of MVO2 indicators and diastolic function. METHODS. 28 consecutive patients with residual angina after PCI were randomized to ivabradine 5 mg twice/day(IG) or standard therapy(CG). All patients performed a stress echocardiography at the enrollment and after 30 days. Myocardial oxygen consumption was estimated from: double product(DP); triple product(TP) integrating DP with ejection-time(ET). Diastolic function was evaluated determining E and A waves, E' measurements and E/E' ratio both at rest and at the peak of exercise.

Conditions

Interventions

TypeNameDescription
DRUGIvabradineIvabradine 5 mg twice a day

Timeline

Start date
2015-03-05
Primary completion
2017-03-07
Completion
2017-03-07
First posted
2019-03-07
Last updated
2019-03-07

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03866395. Inclusion in this directory is not an endorsement.