Whole Blood Platelet Aggregation in Chronic Kidney Disease Patients on Aspirin Study
Completed · Phase 1
Conditions studied: Chronic Kidney Disease
In brief
Higher coronary in-stent thromboses and bleeding complications on anti-platelet agents are more common in Chronic Kidney Disease vs. non-Chronic Kidney Disease patients. Poor inhibition of platelet aggregation by anti-platelet agents predicts future cardiovascular events. Clinical practice guidelines are ambiguous about the use of these agents in Chronic Kidney Disease due to lack of controlled studies. The investigators hypothesize that patients with Chronic Kidney Disease compared with non-Chronic Kidney Disease have reduced platelet aggregation and poor platelet inhibitory response to aspirin. The aims are to 1) define the range of whole blood platelet aggregation in stages 3-5 Chronic Kidney Disease patients; 2) investigate whether patients with stages 4-5 Chronic Kidney Disease vs. non-Chronic Kidney Disease have lower platelet aggregation or impaired von Willebrand Factor activity; and 3) compare inhibition of platelet aggregation from baseline after 2 weeks of aspirin therapy and another 2 weeks of clopidogrel therapy added to aspirin in Chronic Kidney Disease vs. non-Chronic Kidney Disease patients. Accomplishing these aims will provide pilot data to power future studies of targeted anti-platelet agent treatments in Chronic Kidney Disease in order to improve cardiovascular outcomes.
Key facts
- Study ID
- NCT01768637
- Run by
- University of Texas Southwestern Medical Center
- People needed
- 48
- Starts
- 2013-01-01
- Expected to finish
- 2014-06-01
- Last updated by the study team
- 2019-04-19
Who can join
Age: 21 and older, up to 90. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male or female >21 years
- Cases:
- Chronic kidney disease stages 4-5, with estimated glomerular filtration rate of <30
- Controls:
- estimated glomerular filtration rate of >90, urinary albumin to creatinine ratio <30 and no other kidney damage
You may not qualify if…
- End-stage renal disease (peritoneal dialysis and hemodialysis)
- Kidney transplant or any other transplant patient
- Recent hospitalizations <3 months
- Acute coronary or cerebrovascular event in the last 12 months
- Surgery in the last 3 months
- Blood dyscrasias or active bleeding
- Gastro-intestinal bleeding in the last 6 months
- Concomitant use of other anti-platelet agent or antithrombotic drugs
- Recent treatment (<30 days) with a glycoprotein antagonist or proton pump inhibitor
- Hematocrit <25% or white blood cell count >20,000 or platelet count <50,000
- Any active malignancy or liver disease
- No current diagnosis of depression, not on any antidepressant medications,
Where it is running
- University of Texas Southwestern Medical Center — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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