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Cilostazol trial

Cilostazol trial - Cilostazol trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001198
Enrollment
80
Registered
2008-06-20
Start date
2004-10-01
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

peripheral arterial disease

Interventions

Aspirin 81-100mg/day Aspirin 81-100mg/day + cilostazol 200mg/day

Sponsors

Kokura Memorial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)PAD patients with intermittent claudication who had a de novo femoropopliteal disease without an inflow lesion (aortoiliac or common femoral lesion), with an outflow artery (below the knee arteries) with more than one vessel run-off, and with symptoms that were not improved by pharmacotherapy or exercise therapy 2) ankle-brachial index (ABI) of ≤ 0.9 3) a percentage stenosis diameter of ≥ 50% by visual estimate on angiography

Exclusion criteria

Exclusion criteria: previous lower extremity bypass surgery, previous EVT in the femoropopliteal artery, acute onset limb ischemia, or severe lower extremity ischemic symptoms classified into Rutherford Category 4, 5 or 6, known bleeding diathesis, hepatic dysfunction, active gastrointestinal bleeding or peptic ulcer disease, intolerance to cilostazol, aspirin or ticlopidine, pregnant women and women of child-bearing potential, and major life-threatening illness.

Design outcomes

Primary

MeasureTime frame
target vessel revascularization

Secondary

MeasureTime frame
major adverse cardiovascular event, restenosis rate

Countries

Japan

Outcome results

None listed

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