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Do Xanthine Oxidase Inhibitors (XOI) have clinically useful anti-ischaemic effects in the treatment of angina pectoris? A double-blind, placebo controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN82040078
Enrollment
60
Registered
2007-06-26
Start date
2007-06-22
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease - patients with chronic stable angina Circulatory System Coronary Artery Disease

Interventions

Drug: allopurinol 300 mg - 600 mg given for six weeks. Allopurinol (the intervention drug) is given orally (p.o.). Starting dose is 100 mg once daily (od). This is escalated over two weeks to a maxi

Sponsors

University of Dundee (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Documented Coronary artery Disease (CAD) on angiography 2. Chronic stable angina (greater than two months) 3. Able to do Exercise Treadmill Test (ETT) 4. Aged between 30 and 85 years

Exclusion criteria

Exclusion criteria: 1. Contra-indication or unable to do ETT 2. Already on allopurinol or previous allergy to allopurinol 3. Left Ventricular (LV) ejection fraction less than 45% 4. Myocardial Infarction (MI) or Acute Coronary Syndrome (ACS) over the last two months 5. Change to anti-anginal therapy over the last month 6. Percutaneous Coronary Intervention (PCI) or Coronary Artery Bypass Graft (CABG) within the last six months 7. Significant renal or hepatic impairment 8. On medication that may interact with allopurinol (e.g., warfarin)

Design outcomes

Primary

MeasureTime frame
Time to ST depression on ETT. Outcomes will be assessed at the start and every six weeks (at the end of each treatment period - allopurinol or placebo).

Secondary

MeasureTime frame
1. Total exercise time 2. Time to symptom on ETT 3. Assessment of angina 4. Measurement of C-Reactive Protein (CRP), B-type Natriuretic Peptide (BNP) and Procollagen III N-terminal Peptide (PIIINP) Outcomes will be assessed at the start and every six weeks (at the end of each treatment period - allopurinol or placebo).

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026