Personalised Antiplatelet Therapy for Patients With Symptomatic Peripheral Arterial Disease
NCT ID: NCT06047002
Last Updated: 2023-09-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
150 participants
OBSERVATIONAL
2022-09-29
2024-12-31
Brief Summary
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Detailed Description
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In some patients, these two tablets are not effective as expected, because of interactions with other medications they are on or because their bodies cannot process them. This is known as resistance to antiplatelet therapy.
The main aim of this study is to establish how common resistance to aspirin and clopidogrel is in patients with peripheral arterial disease.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients with severely symptomatic aorto-iliac and infra-inguinal peripheral arterial disease.
* Patients with the ability to provide written informed consent.
* Patients on antiplatelet therapy
Exclusion Criteria
* Patients unable or unwilling to provide written informed consent.
* Patients with acute limb ischaemia of the lower limb.
* Patients with aneurysmal disease of the arteries of the lower limb.
* Patients with severe diabetic foot sepsis.
* Patients with a known history of clotting disorders
* Patients with inherited bleeding disorders
18 Years
ALL
No
Sponsors
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University of Leicester
OTHER
Responsible Party
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Principal Investigators
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Sarah Jane Messeder, MBChB
Role: PRINCIPAL_INVESTIGATOR
University of Leicester
Locations
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University Hospitals Leicester
Leicester, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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0829
Identifier Type: -
Identifier Source: org_study_id
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