Prevalence of Aspirin Resistance in Chronic Kidney Disease Patients
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Purpose
The primary objective of the study is to determine the prevalence of aspirin resistance in chronic kidney disease patients. The secondary objectives are to determine possible risk factors contributing to aspirin resistance in this population.
| Condition |
|---|
|
Chronic Kidney Disease |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Cross-Sectional |
| Official Title: | Prevalence of Aspirin Resistance in Chronic Kidney Disease Patients |
- prevalence of aspirin resistance in chronic kidney disease patients [ Time Frame: 2 years ] [ Designated as safety issue: No ]Blood drawn for the Accumetric test
- risk factors contributing to aspirin resistance in this population. [ Time Frame: 2 years ] [ Designated as safety issue: No ]risk factors
Biospecimen Retention: Samples Without DNA
Blood draw
| Enrollment: | 15 |
| Study Start Date: | April 2010 |
| Study Completion Date: | March 2012 |
| Primary Completion Date: | March 2012 (Final data collection date for primary outcome measure) |
A cross-sectional of "aspirin resistance in hemodialysis patients" previously done in our institution showed that 23/66 (34.7%) hemodialysis patients were aspirin resistant. In a recent systematic review, renal impairment was associated with aspirin resistance . This association was seen in only two out of the twenty studies used in this meta-analysis . Both these studies are from the same center with a predominant Asian population. In this study we will try to evaluate the prevalence of aspirin resistance in CKD patient without being limited to a specific ethnicity.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients presenting to the nephrology clinic at SIUH and the nephrology clinic at Staten Island rehab and the admitted patients who give consent.
Inclusion Criteria:
- Patients with known structural kidney disease as evident by history or by urinalysis and CKD stage III or IV determined by MDRD formula and who are taking aspirin.
Exclusion Criteria:
- Younger than 18 years of age.
- Bleeding disorder or myeloproliferative disorders.
- Thrombocytopenia with platelets < 100.000.
- Malignancy.
- Acute hemorrhagic disease.
- A recent history of receipt of platelet glycoprotein IIb/IIIa blockers.
- Liver disease as evident by abnormal liver function and total bilirubin > 2mg/dl.
- use of anticoagulation.
Contacts and Locations| United States, New York | |
| staten island University Hospital nephrology clinic | |
| Staten Island, New York, United States, 10305 | |
| Principal Investigator: | Suzanne El_Sayegh, MD | Staten Island University Hospital |
More Information
No publications provided
| Responsible Party: | Suzanne El-Sayegh, Nephrology Attending, Assoc. Chair of Medicine, North Shore Long Island Jewish Health System |
| ClinicalTrials.gov Identifier: | NCT01364779 History of Changes |
| Other Study ID Numbers: | 10-025 |
| Study First Received: | May 27, 2011 |
| Last Updated: | May 14, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by North Shore Long Island Jewish Health System:
|
aspirin Chronic kidney disease |
Additional relevant MeSH terms:
|
Kidney Diseases Renal Insufficiency, Chronic Kidney Failure, Chronic Urologic Diseases Renal Insufficiency Aspirin Anti-Inflammatory Agents, Non-Steroidal Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions |
Anti-Inflammatory Agents Therapeutic Uses Antirheumatic Agents Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Cardiovascular Agents Hematologic Agents Platelet Aggregation Inhibitors Cyclooxygenase Inhibitors Enzyme Inhibitors Antipyretics Central Nervous System Agents |
ClinicalTrials.gov processed this record on May 21, 2013