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Combined Therapeutic Effect of Probucol and Cilostazol on Endothelial Function in Patients with Silent Cerebral Lacunar Infarcts and Hypercholesterolemia

Combined Therapeutic Effect of Probucol and Cilostazol on Endothelial Function in Patients with Silent Cerebral Lacunar Infarcts and Hypercholesterolemia - Probucol, cilostazol and endothelial function in SLCI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1091220138
Enrollment
20
Registered
2013-09-12
Start date
2011-03-01
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

Investigating the effect of combined therapy with probucol and cilostazol on endothelial function in patients with cerebral infarction and hypercholesterolemia.

Interventions

Intervention type:DRUG Name of intervention: combined therapy with probucol and cilostazol Dose form / Japanese Medical Device Nomenclature:TABLET Route of administration / Site of application:ORAL Do
cilostazol 200mg daily mg Dosing frequency / Frequency of use:BID probucol,500mg
cilostazol 200mg daily Planned duration of intervention:4 weeks Intended dose regimen:probucol,500mg
cilostazol 200mg daily detailes of teratment arms:the patients with silent lacunar cerebral infarcts and mild hypercholesterolemia Comparative intervention name:aspirin (100 mg/day) prescription group

Sponsors

Takase Bonpei
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: lacunar cerebral infarct diagnosed by MRI and hypercholesterolemia (LDL >140mg/gL)

Exclusion criteria

Exclusion criteria: allergic reaction to probucol, cilostazol, or aspirin or any other acute and/or severe disorders

Design outcomes

Primary

MeasureTime frame
endothelial function

Secondary

MeasureTime frame
Presence of side effect

Countries

Japan

Contacts

Public ContactTakase Bonpei

National Defense Medical College

bonpeit@ndmc.ac.jp+81-4-2994-1511

Outcome results

None listed

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