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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01364779
Other study ID # 10-025
Secondary ID
Status Completed
Phase N/A
First received May 27, 2011
Last updated May 14, 2013
Start date April 2010
Est. completion date March 2012

Study information

Verified date May 2013
Source Northwell Health
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date March 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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.

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Locations

Country Name City State
United States staten island University Hospital nephrology clinic Staten Island New York

Sponsors (2)

Lead Sponsor Collaborator
Northwell Health Staten Island University Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary prevalence of aspirin resistance in chronic kidney disease patients Blood drawn for the Accumetric test 2 years No
Secondary risk factors contributing to aspirin resistance in this population. risk factors 2 years No
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