Clinical Trials Directory

Trials / Completed

CompletedNCT05247385

Platelet Aggregation and Adenosine Levels Among Patients Taking Ticagrelor or Prasugrel

Platelet Aggregation and Adenosine Levels Among Patients With Stable Chronic Coronary Artery Disease Taking Ticagrelor or Prasugrel

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
87 (actual)
Sponsor
University of Sao Paulo · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

Prospective, single-center, double blind, double dummy, randomized trial. Platelet function tests and adenosine levels were assessed at baseline and 15 days after taking Ticagrelor with Prasugrel placebo or Prasugrel with Ticagrelor placebo in stable patients with coronary artery disease

Detailed description

This was a prospective, double blinded, randomized trial that compared platelet inhibition and adenosine levels with ticagrelor (180mg loading dose, followed by 90 mg BID) versus prasugrel (60mg loading dose, followed by 10 mg QD) . Patients were eligible if they were between 18 and 75 years old, were on aspirin without P2Y12 inhibitor at baseline and \> 1 year after documented ACS. Platelet aggregation was compared with the Multiplate ADP® assay, performed at baseline and after 15 days on study medication. Adenosine plasma levels were measured with high performance liquid chromatography at the same time points

Conditions

Interventions

TypeNameDescription
DRUGPrasugrelCompared platelet inhibition and adenosine levels at baseline and after 15 days
DRUGTicagrelorCompared platelet inhibition and adenosine levels at baseline and after 15 days

Timeline

Start date
2017-03-20
Primary completion
2021-02-26
Completion
2021-12-20
First posted
2022-02-18
Last updated
2022-02-18

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT05247385. Inclusion in this directory is not an endorsement.