Allopurinol in Acute Coronary Syndrome
Launched by STEPHEN MCSWIGGAN · Oct 20, 2011
Trial Information
Current as of August 11, 2025
Terminated
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • angiographically documented coronary artery disease,
- • a positive exercise tolerance test (ETT)
- • a history of symptoms of chronic, stable, effort-induced angina for ≥ 2 months.
- • All concomitant antianginal medication will be allowed and continued unchanged during the study.
- Exclusion Criteria:
- • the inability to do an ETT due to back or leg problems,
- • myocardial infarction or acute coronary syndrome ≤ 2 months,
- • coronary revascularization (percutaneous or CABG) ≤ 6 months,
- • Left Ventricular Ejection Fraction \<45%,
- • estimated GFR \<60 ml/min or creatinine \>180 mmol/ml,
- • significant valvular pathology,
- • already had gout or on allopurinol,
- • atrial arrhythmias or ECG abnormalities interfering with ST-segment interpretation,
- • previous ventricular arrhythmias on ETT,
- • severe hepatic disease
- • or on azathioprine, 6 mercaptopurine or warfarin.
- • Patients who have participated in any other clinical trial within the previous 30 days will be excluded.
- • Patients who are unable to give informed consent will also be excluded from this trial
About Stephen Mcswiggan
Stephen McSwiggan is a dedicated clinical trial sponsor with a commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and rigorous scientific methodologies, McSwiggan oversees the design, implementation, and management of clinical trials across various therapeutic areas. His expertise lies in fostering collaboration among multidisciplinary teams, ensuring compliance with regulatory standards, and promoting ethical practices throughout the research process. Through strategic partnerships and a patient-centered approach, Stephen McSwiggan aims to facilitate the development of groundbreaking treatments that address unmet medical needs.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Dundee, Angus, United Kingdom
Patients applied
Trial Officials
Allan Struthers, BSc, MD, FRCP, FRSE, FMedSci
Principal Investigator
University of Dundee
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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