Viewing Study NCT03150667



Ignite Creation Date: 2024-05-06 @ 10:04 AM
Last Modification Date: 2024-10-26 @ 12:24 PM
Study NCT ID: NCT03150667
Status: UNKNOWN
Last Update Posted: 2018-05-25
First Post: 2017-05-05

Brief Title: Study Comparing Treatment Effectiveness of Guideline Indicated APT for ACS in Patients With CKD
Sponsor: North Texas Veterans Healthcare System
Organization: North Texas Veterans Healthcare System

Study Overview

Official Title: Pragmatic Randomized Controlled Trial Comparing Treatment Effectiveness of Guideline Indicated Anti-platelet Therapy for Acute Coronary Syndrome in Patients With Chronic Kidney Disease
Status: UNKNOWN
Status Verified Date: 2018-05
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CPRS-CKD
Brief Summary: To compare clinical outcomes in patients with chronic kidney disease CKD presenting with an acute coronary syndrome ACS treated with clopidogrel or ticagrelor both FDA approved and guideline indicated drugs for treating these patients upstream managed medically or with coronary revascularization
Detailed Description: The purpose of this trial is to see if ticagrelor is a better antiplatelet treatment option than clopidogrel for dual antiplatelet therapy with aspirin in chronic kidney disease CKD patients presenting with acute coronary syndrome ACS This study will be a comparative effectiveness trial of the two guideline-based treatments for patients with ACS with CKD who are at a significantly higher risk of mortality and morbidity and often receive sub-optimal treatment Ticagrelor and clopidogrel are the only two drugs in ACS that are approved for upstream on admission use both in CKD and non-CKD patients who are managed both medically conservatively or with coronary revascularization with PCI-percutaneous coronary revascularization or CABG-coronary artery bypass graft surgery Both of these drugs are not cleared renally and do not require dose adjustments in any stage of CKD

Moreover as a significant majority of CKD patients presenting with ACS are initially cared for by internists hospitalists and nephrologists execution of this study at VA hospitals will strengthen collaboration between these specialties with cardiology and help adopt best practice pathways across multiple services participating in the care of this high-risk patient population Finally the study and its findings will for the first time provide randomized clinical trial evidence to guide the care of CKD patients with ACS who are at a high risk for both recurrent ischemia and bleeding complications

Hypothesis to be tested The Investigators hypothesize that use of guideline-indicated dual antiplatelet therapy DAPT with ticagrelor compared to clopidogrel in CKD patients presenting with ACS will reduce ischemic cardiovascular events at 1 year additionally without a significant increase in severe bleeding Bleeding Associated Research Consortium or BARC 3 category over the same period This hypothesis is based on prior subgroup analysis of published studies

Randomized patients will be followed for 1 year from date of admission and events recorded through chart review For patients who are event free a phone follow-up will be done at the end of 1 year to note events which will be recorded on the medical chart as well

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None