Allopurinol as a Possible Oxygen Sparing Agent During Exercise in Peripheral Arterial Disease
NCT01147705 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2017-05-02
Summary
Peripheral arterial disease (PAD) is a common condition that arises due to the build up of atheroma in the arteries supplying blood to the peripheral muscles and other tissues. This imbalance between oxygen supply and demand becomes particularly apparent when patients with the condition are walking. The pain and weakness they experience (mainly in the calf but less commonly in the thigh) is known as intermittent claudication and resolves upon cessation of exercise.
It is an important disease to study as it is (i) common (est. prevalence of symptomatic intermittent claudication in Scotland of 4.5%) and (ii) those with it have a 1.6 times higher relative risk of ischaemic heart disease. These patients also have a significantly higher mortality than age-matched controls at around 12% per year.
There are two main aims of therapy - (i) to reduce the risk of cardiovascular events by way of standard secondary prevention measures (smoking cessation, anti-platelet, anti-hypertensive and cholesterol-lowering therapy, diabetic control) and (ii) to treat symptoms.
Supervised exercise therapy has been shown to be beneficial in improving walking time and distance in selected patients with leg pain from intermittent claudication with an overall increase in walking distance of approximately 150 metres at three months.
There are numerous drug treatments available for consideration in PAD patients (mainly cilostazol in the UK), but many of these have either undesirable side effects or no clear evidence of benefit. The range of increase in walking distance on cilostazol was reported to be a 50-76% increase over three months compared to 20% with placebo with some significant improvements in Quality of Life (QOL) indicators, although with a significant number of adverse effects (16% vs 8% on placebo) limiting therapy. The current cost (March 2010) is £35.31/month.
Other options for therapy include angioplasty and bypass surgery. At present these are only recommended for patients who fail to respond to medical therapy and have severely disabling symptoms (in the absence of significant exercise-limiting comorbidities).
Conditions
- Peripheral Arterial Disease
Interventions
- DRUG
-
Allopurinol
Participants will be given blinded medication and asked to take one tab/day for the first six weeks (100mg strength for two weeks then 300mg strength for four weeks) followed by two tabs/day for the remaining 18 weeks
- DRUG
-
Same appearance/dosing as active drug.
Sponsors & Collaborators
-
NHS Tayside
collaborator OTHER_GOV -
British Heart Foundation
collaborator OTHER -
University of Dundee
lead OTHER
Principal Investigators
-
Allan Struthers, MD FRCP · University of Dundee
-
Alan J Robertson, MBChB MRCP · University of Dundee
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 35 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-02-28
- Primary Completion
- 2012-07-31
- Completion
- 2012-07-31
Countries
- United Kingdom
Study Locations
More Related Trials
-
APEX Study: Effects of Allopurinol on Coronary and Peripheral Endothelial Function in Patients With Cardiac Syndrome X
NCT00512057 ·Status: COMPLETED ·Phase: PHASE4
-
Effects of Allopurinol on Inflammation and Ultrasonographic Changes in People With Elevated Uric Acid But no Symptoms
NCT04012294 ·Status: UNKNOWN ·Phase: PHASE3
-
Sex-related Differences in Arterial Stiffness in Type 2 Diabetics: Role of Uric Acid
NCT03648996 ·Status: COMPLETED ·Phase: PHASE2
-
Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion
NCT02752633 ·Status: COMPLETED ·Phase: PHASE4
-
Uric Acid and Hypertension in African Americans
NCT00241839 ·Status: COMPLETED ·Phase: PHASE3
-
Allopurinol in Acute Coronary Syndrome
NCT03745729 ·Status: COMPLETED ·Phase: PHASE4
-
Allopurinol in Functional Impairment (ALFIE) Trial: 'Improving Muscle Strength'
NCT01550107 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation of PK and Safety of D-0120 and Allopurinol
NCT05360628 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Allopurinol in Acute Gout
NCT01775098 ·Status: WITHDRAWN ·Phase: NA
-
Does Allopurinol Prolong a Treated, Acute Gout Flare?
NCT01988402 ·Status: COMPLETED ·Phase: PHASE4
-
Uric Acid and the Endothelium in CKD
NCT01228903 ·Status: COMPLETED ·Phase: NA
-
Center of Research Translation (CORT) Project 2
NCT02038179 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Primary Prevention of Hypertension in Obese Adolescents
NCT00288158 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ABP-671 in Healthy Subjects
NCT03906006 ·Status: COMPLETED ·Phase: PHASE1
-
PREventative Study Against URate-lowering Drug-induced Gout Exacerbations 1
NCT00829829 ·Status: COMPLETED ·Phase: PHASE3
-
The Effects of BCRP Q141K on Allopurinol Pharmacokinetics and Dynamics
NCT02956278 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Febuxostat Effect on Blood Pressure in Patients With High Normal Blood Pressure
NCT01472692 ·Status: COMPLETED ·Phase: PHASE4
-
Allopurinol in Patients With Refractory Angina to Improve Ischemic Symptoms
NCT04368819 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Initiation of Allopurinol at First Medical Contact for Acute Attacks of Gout
NCT01310673 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Evaluate ALN-XDH in Healthy Subjects and Patients With Gout
NCT05256810 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Effect of Allopurinol on Markers of Mineral and Bone Metabolism
NCT05601271 ·Status: COMPLETED ·Phase: NA
-
Prednisone for Heart Failure Patients With Hyperuricemia
NCT02129764 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Investigation of the Atherogenic Effects of Uric Acid-modified in Endothelial Dysfunction and the the Preventional Mechanism by Anthocyanidines
NCT02797028 ·Status: UNKNOWN ·Phase: PHASE4
-
Microalbuminuria and Allopurinol in Type 1 Diabetes
NCT02829177 ·Status: COMPLETED ·Phase: PHASE4
-
Optimal Administration of Allopurinol in Dialysis Patients
NCT02477488 ·Status: COMPLETED ·Phase: PHASE4