Study Comparing Treatment Effectiveness of Guideline Indicated APT for ACS in Patients With CKD
Status unconfirmed · Phase 4
Conditions studied: Chronic Kidney Diseases, Acute Coronary Syndrome
In brief
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).
Key facts
- Study ID
- NCT03150667
- Run by
- North Texas Veterans Healthcare System
- People needed
- 220
- Starts
- 2017-04-10
- Expected to finish
- 2020-04-30
- Last updated by the study team
- 2018-05-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hospital admission with non-emergent ACS qualifying diagnosis: chest pain, unstable angina or NSTEMI
- A decision to prescribe clopidogrel or ticagrelor in addition to aspirin (DAPT-dual antiplatelet therapy) by the attending physician
- A eGFR< 60 mL/min per 1.73 m.2 (as defined in the EMR or CPRS reported results)
You may not qualify if…
- Diagnosis of ST Elevation Myocardial Infarction (STEMI) at admission
- History of intra-cranial hemorrhage
- Bleeding requiring hospitalization, surgery, or transfusion within the past 3 months
- Life expectancy in the opinion of the provider < 6 months
- Chronic antithrombotic therapy
- Known allergy to clopidogrel or ticagrelor
- Patients on hemodialysis
Where it is running
- Durham VA Medical Center — Durham, North Carolina, United States (enrolling)
- VA North Texas Health Care System — Dallas, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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