Skip to content

The effect of the cognitive function and cerebral white matter lesions of pitavastatin in hypercholesterolemic patients with cognitive dysfunction.

The effect of the cognitive function and cerebral white matter lesions of pitavastatin in hypercholesterolemic patients with cognitive dysfunction. - the effect on the cognitive function and cerebral white matter lesions of pitavastatin in hypercholesterolemic patients with cognitive dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013231
Enrollment
60
Registered
2014-03-01
Start date
2014-03-01
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

Hypercholesterolemic patients with cognitive dysfunction

Interventions

Pitavastatin Calcium(LIVALO) Taking a dose of 1-4mg once daily. Daily dose is determined based on Japan Atherosclerosis Society Guidelines 2012 for Prevension of Atherosclerotic Cardiovascular Diseas

Sponsors

Department of Geriatric Medicine, Kyorin University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Outpatients of Kyorin University Hospital Amnesia Center Judged that a lipid-lower therapy is required by Japan Atherosclerosis Society Guidelines 2012 for Prevention of Atherosclerotic Cardiovascular Diseases over 65 years old. 2.Patients who receive any statin can entry after 4 weeks washout periods. 3.the mild cognitive impairment to dementia patients.(15<=MMSE<=30) 4.PVH grade >=1/4 or DWMH grade >=1/4 (judged by two or more doctors) 5.Written informed consent is obtained from subjects or their family relatives or legally acceptable representatives before entry.

Exclusion criteria

Exclusion criteria: 1.History of hypersensitivity to any of the ingredients of the product. 2.Severe hepatic disorder or biliary atresia. 3.Receiving cyclosporine. 4.Patients receiving fibrates who also have laboratory evidence of abnormal renal function. 5.Individuals who are ineligible in the opinion of the physician in charge.

Design outcomes

Primary

MeasureTime frame
.Change of cerebral white matter lesions(MRI) .Change of arteriosclerosis marker(PWV, IMT) .Change of cognitive function(MMSE) .Change of cerebral blood flow(SPECT) .Change of serum lipids

Countries

Japan

Contacts

Public ContactYukiko Moriya

Kyorin University School of Medicine Department of Geriatric Medicine

m-yukiko@rk9.so-net.ne.jp0422-47-5511

Outcome results

None listed

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