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Efficacy and Safety of Cilostazol in Patients of Vascular Cognitive Impairment-no Dementia (VCIND)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01872858
Enrollment
200
Registered
2013-06-07
Start date
2010-11-30
Completion date
2015-11-30
Last updated
2013-06-07

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

Conditions

Mild Cognitive Impairment

Brief summary

Patients of vascular cognitive impairment-no dementia (VCIND) in one group is prescribed cilostazol,in the other group is prescribed aspirin. Evaluate both of them in cognitive function, MRI and other sides at given time. The investigators hypothesize that cilostazol is more efficient and safer than aspirin in patients with VCIND.

Interventions

DRUGAspirin

Aspirin, 100mg, Q.D, p.o, 2yr

DRUGCilostazol

cilostazol, 100mg, B.I.D, p.o, 2yr

Sponsors

Huashan Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Aged between 50-80, both gender; 2. Small vessel disease and associated cognitive impairment, diagnosed as VCIND; 3. Non-specific subjective symptoms (dizziness, somnolence, numbness in limbs) are acceptable. 4. Normal hepatic and renal function. 5. With good compliance.

Exclusion criteria

1. Aged above 80 or less than 50. 2. Dementia. 3. Cerebral infarction(\>2cm). 4. Major vascular lesion. (stenosis\>50%). 5. Cardiac cerebral infarction. 6. Intracerebral Hemorrhage. 7. Clinical manifestations cannot attribute to small vessel disease. 8. Major depression or dysfunction in speech, visual ability, hearing or aphasia that would interfere with the cognitive assessment. 9. Severe systematic organic impairment(cardiac, hepatic, renal dysfunction). 10. Thrombocytopenic Purpura. 11. History of hemorrhage in digestive system or surgery in past 3 months. 12. Previously on cilostazol treatment for more than 3 month. 13. Allergic to aspirin or cilostazol. 14. Enrolled in other clinical trials in past 3 months. 15. Lack of informed consent or compliance. 16. Contraindications for MRI scan.

Design outcomes

Primary

MeasureTime frameDescription
changes in cognitive functionbaseline, 3month, 6month, 1year, and 2yearscores in Montreal Cognitive Assessment,Mini-Mental Status Examination, Clinal Dementia Rating,trail making test, similarity test, Stroop test.

Secondary

MeasureTime frameDescription
Number of Participants with Incident cerebral vascular event3month, 6month, 1year and 2yearincluding cerebral infarct, cerebral hemorrhage, transient ischemic attack.
Changes of peripheral inflammatory markers levelbaseline, 2yearintercellular adhesion molecules(ICAM), thrombomodulin, tissue factor(TF), tissue factor plasma inhibitor,TFPI, etc.
The progression of cerebral white matter lesion and lacunar infarctionbaseline, 3month, 6month, 1year and 2year
changes in MRI-diffused tension image(DTI)baseline, 2yearcerebral volume , lacune infarct, white matter lesion, micro-bleed, apparent diffusion coefficient(ADC) .

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026