- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00327041
Monitoring Response to Antiplatelet Therapy
Pilot Study Investigating the Use of a Variety of Assays to Detect Individual Response to Antiplatelet Therapy
Study Overview
Status
Study Type
Enrollment
Contacts and Locations
Study Contact
- Name: Richard IS Good, BA MBBS MRCP
- Phone Number: 0044 141 211 6390
- Email: richard_good@hotmail.com
Study Contact Backup
- Name: Keith G Oldroyd, MBChB, MD, FRCP
- Phone Number: 0044 141 211 2337
- Email: keith.Oldroyd@northglasgow.scot.nhs.uk
Study Locations
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Scotland
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Glasgow, Scotland, United Kingdom, G11 6NT
- Recruiting
- Western Infirmary
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Patients aged 18-80 undergoing intended PCI for conventional indications. Informed written consent.
Exclusion Criteria:
Administration of GPIIbIIIa therapy prior to PCI, Oral anticoagulation, ticlopidine, dipyridamole, NSAID therapy, Pregnancy, Troponin I >0.2mcg/l on day of procedure, Chest pain in the 24 hrs prior to PCI. Anaemia (Hb<10g/dl). Platelet Count <150 or >450 x10^9/l, Personal or family history of bleeding disorder.
Study Plan
How is the study designed?
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Keith G Oldroyd, MBChB, MD, FRCP, NHS Greater Glasgow and Clyde
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- rgoodtrial001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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