Aspirin to Target Arterial Events in Chronic Kidney Disease

NCT03796156 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 4633

Last updated 2026-03-20

No results posted yet for this study

Summary

This study aims to find out whether people with chronic kidney disease \[CKD\] should take low dose aspirin to reduce the risk of first heart attack or stroke (cardiovascular disease \[CVD\]). CKD is common and is associated with an increased risk of CVD.

CVD is caused by small blood clots and aspirin thins the blood to reduce the risk of such clots developing but it also increases the risk of bleeding.

Aspirin is recommended to prevent further CVD in people who have already had a first CVD event (so called secondary prevention). Here the investigators want to study the use of aspirin as primary prevention in people with CKD who have not had a CVD to prevent the first event, to assess whether the potential benefits exceed the risks.

Eligible patients will be recruited from their United Kingdom (UK) general practices and allocated by chance to be prescribed once daily low dose aspirin or usual care only. Follow-up will be for several years both electronically (for general practice, hospital and mortality data) and by annual questionnaires to ascertain CVD and bleeding events.

Conditions

Interventions

DRUG

Aspirin

75mg low dose non enteric coated or dispersible

Sponsors & Collaborators

  • University of Nottingham

    collaborator OTHER
  • University of Warwick

    collaborator OTHER
  • Nottingham University Hospitals NHS Trust

    collaborator OTHER
  • East Kent Hospitals University NHS Foundation Trust

    collaborator OTHER_GOV
  • University of Durham

    collaborator OTHER
  • Epsom and St Helier University Hospitals NHS Trust

    collaborator OTHER
  • University of Southampton

    lead OTHER

Principal Investigators

  • Hugh Gallagher, MD · Epsom and St Helier University Hospitals NHS Trust

  • Simon Fraser, MD · University of Southampton

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-25
Primary Completion
2024-09-30
Completion
2025-09-23

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03796156 on ClinicalTrials.gov