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clOpidogrel resIstaNce in a Selected Population of Patients at a Tertiary Cardiovascular Center in Trinidad - Trial NCT03667066

Access comprehensive clinical trial information for NCT03667066 through Pure Global AI's free database. This phase not specified trial is sponsored by The University of The West Indies and is currently Completed. The study focuses on Platelet Dysfunction. Target enrollment is 40 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT03667066
Completed
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Trial Details
ClinicalTrials.gov โ€ข NCT03667066
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clOpidogrel resIstaNce in a Selected Population of Patients at a Tertiary Cardiovascular Center in Trinidad
Prevalence of clOpidogrel resIstaNce in a Selected Population of Patients Undergoing Elective Percutaneous Coronary Intervention at a Tertiary Cardiovascular Center in Trinidad: The POINT Pilot Study

Study Focus

Platelet Dysfunction

Clopidogrel

Observational

drug

Sponsor & Location

The University of The West Indies

Port Of Spain, Trinidad and Tobago

Timeline & Enrollment

N/A

Sep 01, 2017

Jun 01, 2018

40 participants

Primary Outcome

Overall prevalence of HPR in the Trinidadian population undergoing elective percutaneous coronary intervention

Summary

The aim of this study was to determine the prevalence of clopidogrel resistance among a
 selected group of patients undergoing elective percutaneous coronary intervention and to
 observe whether there was any south-Asian (Indo-Trinidadian) predilection for HPR considering
 the well-established epidemiologic trends for accelerated CAD within this subgroup.

ICD-10 Classifications

Qualitative platelet defects
Antithrombotic drugs [platelet-aggregation inhibitors]
Essential (haemorrhagic) thrombocythaemia
Other thrombophilia
Haemorrhagic disorder due to circulating anticoagulants

Data Source

ClinicalTrials.gov

NCT03667066

Non-Device Trial