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Study on diagnosis of Alzheimer disease by amyloid imaging: A multi-center trial

Study on diagnosis of Alzheimer disease by amyloid imaging: A multi-center trial - A PET study of amyloid imaging in Alzheimer disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000000558
Enrollment
80
Registered
2007-01-10
Start date
2006-10-01
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

Healthy normal volunteers, Mild cognitive impairment (MCI), Alzheimer disease (AD)

Interventions

None listed

Sponsors

Study Group on diagnosis of Alzheimer disease by amyloid imaging using [11C]BF-227
Lead Sponsor
1)Department of Geriatrics and Gerontology, Tohoku University School of medicine 2)Cyclotron and Radioisotope Center, Tohoku University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Criteria for Normal volunteers: Normal Volunteers are examined by FDG-PET, [11C]BF-227-PET, MRI and psychological tests. Male and female volunteers aged more than 35 years old are recruited for this study. They should understand the purpose and rationale of this study. 2)Criteria for Alzheimer disease: Alzheimer patients diagnosed as a probable AD according to NINCDS-ADRDA are enrolled. MMSE (Mini-mental state examination) is over 18, and apparent cognitive dysfunction is present in the patients. Informed consents are obtained from patients family and possibly from patients themselves. 3)Criteria for Mild Cognitive Impairment 1.Amnestic MCI. 2.No apparent neurological and psychiatric disorders. 3.There are no neurological symptoms. 4.There are no psychiatric symptoms. 5.The patients do not show dementia.

Exclusion criteria

Exclusion criteria: 1)The past and present history of alcoholism. 2)The past and present history of epilepsy 3)Education period is less than 6 years. 4)There are no persons who can give any information on patients symptoms. 5)Diabetic patients treated with insulin 6)Patients treated with antidepressants, antipsychotics, and long-term sedative-hypnotics. 7)Severe complication including malignancy, heart failure, hepatic dysfunction, renal dysfunction, endocrine disorders, etc. 8)Other patients and volunteers that investigators and medical doctors need to exclude.

Design outcomes

Primary

MeasureTime frame
The molecular PET imaging using [11C]BF-227. The [11C]BF-227-PET is evaluated by cortical SUV ratios to cerebellum as a reference among healthy volunteers, mild cognitive impairment, and Alzheimer patients.

Secondary

MeasureTime frame
The comparison of FDG-PET, MRI, psychological cognitive tests, and [11C]BF-227-PET among healthy volunteers, mild cognitive impairment, and Alzheimer patients. The [11C]BF-227-PET is evaluated by cortical SUV ratios to cerebellum as a reference

Countries

Japan

Contacts

Public ContactDr. Nobuyuki Okamura

Tohoku University Graduate School of Medicine Department of Pharmacology

yanai@med.tohoku.ac.jp022-717-8058

Outcome results

None listed

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