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Clinical Trials/JPRN-jRCTs051180214
JPRN-jRCTs051180214
Recruiting
未知

The usefulness of brain amyloid image using flutemetamol and glucose metabolism for the neurogenerative disease - The usefulness of brain amyloid image using flutemetamol and glucose metabolism for the neurogenerative disease

Itoh Yoshiaki0 sites100 target enrollmentMarch 27, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Itoh Yoshiaki
Enrollment
100
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 27, 2019
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Itoh Yoshiaki

Eligibility Criteria

Inclusion Criteria

  • Healthy control
  • 1\. Ages 20 and over
  • 2\. Written informed consent
  • 1\. Diagnosed as neurogenerative disease related to tau protain (Alzheimer's disease, Dementia with Lewy Bodies, Frontotemporal lobar degeneration, Parkinson's syndrome) by clinical symptom, Neurological findings, MRI and cognitive function test.
  • 2\. Written informed consent

Exclusion Criteria

  • Healthy control
  • 1\. A person who has brain disease (Parkinson's disease, dementia related disease, etc.)
  • 2\. A person who has serious disease complications or who has a history of these and who is considered as inappropriate by researcher.
  • 3\. Pregnant, unwilling to practice contraception during the study, or lactating female.
  • 4\. Participated in nuclear medicine examination within 6 months.
  • 5\. Claustrophobia
  • 6\. Judged inappropriate as subject by investigator.
  • 1\. A person who is complicated by brain disease other than the disease concerned (including an obvious history of cerebral infarction) and taking a drug that effects on the central nervous system
  • 2\. A person who has serious disease complications or has a history of these and is judged to be unsuitable as a subject of this research by a doctor who is a researcher etc.
  • 3\. Pregnant, unwilling to practice contraception during the study, or lactating female.

Outcomes

Primary Outcomes

Not specified

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