Cilostazol-Aspirin Therapy Against Recurrent Stroke With Intracranial Artery Stenosis

Cerebrovascular Disease Clinical Trial

Official title:

Cilostazol-Aspirin Therapy Against Recurrent Stroke With Intracranial Artery Stenosis (CATHARSIS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00333164
• Other study ID #: UHA STROKE04-01
• Status: Completed
• Phase: Phase 3
• First received: June 1, 2006
• Last updated: December 18, 2017
• Start date: May 2006
• Est. completion date: March 2012

Study information

• Verified date: August 2012
• Source: Translational Research Informatics Center, Kobe, Hyogo, Japan
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Multi-center, open-labelled randomized controlled trial, to study the effect of aspirin plus cilostazol and aspirin alone on the progression of intracranial arterial stenosis, in 200 chronic stroke patients with 50-99% stenosis, to be followed up for 2 years

Description:

Intracraial arterial stenosis (IAS) is more common in Asia, including Japanese, than in Cocasian. Also, stroke recurrence rate is high in patients with such lesions, despite medical treatment. Accoding to the result of WASID (N Engl J Med 2005;352:1305-16), warfarin is not recommended because of the concern of safety (higher risk of intracranial hemorrhage and death when compared with aspirin), wheras the efficacy of aspirin is not enough in symptomatic IAS patients. Under these conditions, we planned to conduct a nationwide multi-center, open labelled, randomized controlled trial to compare the effect of aspirin plus cilostazol (phosphodiestrase type 3 inhibitor) and aspirin alone on the progression of IAS in 200 IAS patients with ischemic stroke after 2 weeks to 6 months of onset. Patients are randomly allocated to either of two groups. Aspirin 100mg/day plus cilostazol 200 mg/day is given to the 100 patients in one group, and aspirin 100 mg/day alone is given to 100 patients in another group.

Follow-up period is at least two years. The primary endpoint is progression of IAS on MRA at two years after randomization. The secondary endpoints are cardiovascular events (ischemic stroke, myocardial infarct, and other vascular events), death, serious adverse events, new silent brain infarcts, and activity of daily life. The purpose of this study is to establish the best medical treatment in symptomatic IAS patients. This study will also provide important information for the future randomized controlled study to compare medical treatment alone and intravascular intervetnion (PTA and/or stenting) in these patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 200
• Est. completion date: March 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 85 Years

Eligibility

Inclusion Criteria:

• (1) Ischemic stroke after two weeks to six months from onset,

• (2) Responsible lesion identified on MRI,

• ( 3) Intracranial arterial stenosis >50% on MRA in the territory of responsible lesion,

• (4) Intracranial arterial stenosis in suproclinoid internal carotid arterry, M1 portion of midlle cerebral artery, or basilar artery,

• (5) Age of 45 to 85 years,

• (6) Able to visit out-patient clinic, and

• (7) Written informed consent obtained from patient or family.

Exclusion Criteria:

• (1) Patients with potential cardiac embolic sources,

• (2) Patients receiving cilostazol,

• (3) Patients on warfarin treatment,

• (4) Patients in whom MRI cannot be perfomed,

• (5) Patients in whom PTA or bypass surgery is planned,

• (6) Patients with history of symptomatic intracranial hemorrhage, other hemorrhagic diseases (active peptic ulcer etc.), hemophilia or coagulation abnormalities,

• (7) Patients with hypersensitivity to cilostazol or aspirin,

• (8) Patients with congestive heart failure or uncontrollable angina pectoris,

• (9) Patients with thrombocytopenia (<100,000/mm3),

• (10) Patients with liver dysfunction (AST or ALT >100 IU/L),

• (11) Patients with renal dysfunction (Creatinin >2.0 mg/dl),

• (12) Patients who cannot to be followed up during the study period,

• (13) Patients who are enrolled in other clinical trials, and

• (14) Patients inadequate for this study by other reasons.

Related Conditions & MeSH terms

• Cerebrovascular Disease
• Cerebrovascular Disorders

Intervention

Drug:
• Asprin, Cilostazol

Locations

Country	Name	City	State
Japan	Tokyo Women's Medical University School of Medicine	Shinjuku-ku	Tokyo

Sponsors (8)

Lead Sponsor	Collaborator
Translational Research Informatics Center, Kobe, Hyogo, Japan	China National Center for Cardiovascular Diseases, Department of Neurology, Saiseikai Central Hospital, Foundation for Biomedical Research and Innovation, Kobe City General Hospital, Kyushu University, Neurology, Tokyo Women's Medical University, School of Medicine, Tohoku University

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression of intracranial arterial stenosis after two years
Secondary	Cardiovascular events (ischemic stroke, cardiac infarctin, and other vascular events ),
Secondary	death (stroke death, vascular death except for stroke ),
Secondary	serious adverse events, new silent brain infarcts, and degrees of activity of daily living.