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Toyama Anti-arteriosclerosis and Plaque Assessment Trial by Aggressive Lipid Lowering Therapy with Pitavastatin in Peripheral Artery Disease

Toyama Anti-arteriosclerosis and Plaque Assessment Trial by Aggressive Lipid Lowering Therapy with Pitavastatin in Peripheral Artery Disease - TULIP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003628
Enrollment
50
Registered
2010-06-01
Start date
2010-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients with peripheral artery disease and hypercholesterolemia

Interventions

intensive lipid lowering therapy with Pitavastatin, 1 to 4mg once daily, to achieve serum LDL cholesterol level less than 80mg/dl. conventional lipid lowering therapy with Pitavastatin, 1 to 4mg once

Sponsors

The Second Department of Internal Medicine, University of Toyama, Graduate school of medicine and pharmaceutical science,
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patient without coronary artery disease, whose LDL cholesterol >= 120mg/dl 2) Patient with coronary artery disease, whose LDL cholesterol >= 100mg/dl 3) Ankle Brachial Pressure Index (ABI) <= 0.9

Exclusion criteria

Exclusion criteria: 1) Following "contraindication" or "essentially contraindication" of pitavastatin as follows: severe liver injury or biliary obstruction patients taking cyclosporin pregnant or possible pregnant women or breast-feeding women patients with renal dysfunction and taking fibrates 2) patients already taking pitavastatin 3) patients with maintenance dialysis 4) patients who plan to undergo or underwent bilateral lower limb revascularization within within 3 months. 5) patients with severe peripheral artery disease (Fontaine classification class 4) 6) patient with previous cerebral hemorrhage 7) patients who judged inadequate by the co-execution doctor

Design outcomes

Primary

MeasureTime frame
claudication time on Treadmill exercise test

Countries

Japan

Contacts

Public ContactTomoki Kameyama

University of Toyama Graduate school of medicine and pharmaceutical science, The Second Department of Internal Medicine

076-434-7297

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026