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A Study Comparing Cardiovascular Effects of Ticagrelor and Clopidogrel in Patients With Peripheral Artery Disease (EUCLID)

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 3

Conditions

Peripheral Artery Disease

Treatments

Drug: Clopidogrel
Drug: Ticagrelor

Study type

Interventional

Funder types

Industry

Identifiers

NCT01732822
D5135C00001
2011-004616-36 (EudraCT Number)

Details and patient eligibility

About

The purpose of this study is to compare the effects of ticagrelor and clopidogrel in patients with Peripheral Artery Disease.

Full description

A randomized, double-blind, parallel group, multicentre phase IIIb study to compare ticagrelor with clopidogrel treatment on the risk of cardiovascular death, myocardial infarction and ischemic stroke in patients with established Peripheral Artery Disease (EUCLID Examining Use of tiCagreLor In paD)

Enrollment

13,885 patients

Sex

All

Ages

50 to 130 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and Female patients 50 years old or older Symptomatic peripheral artery disease

Exclusion criteria

  • Patients needing dual anti-platlet drug treatment before start of study Planned revascularisation or amputation
  • Patients with known bleeding disorders
  • Patients with a history of intracranial bleed
  • Patients considered to be at risk of bradycardic events unless already treated with a permanent pacemaker

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

13,885 participants in 2 patient groups

Ticagrelor
Experimental group
Description:
Ticagrelor 90 mg bd (and Clopidogrel placebo od) taken orally as tablets
Treatment:
Drug: Ticagrelor
Clopidogrel
Active Comparator group
Description:
Clopidogrel 75 mg od (and Ticagrelor placebo bd) taken orally as tablets
Treatment:
Drug: Clopidogrel

Trial contacts and locations

778

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Data sourced from clinicaltrials.gov

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