UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000004326
Receipt number R000005184
Scientific Title Quantification of amyloid deposition using positron emission tomography with [C-11]AZD2184
Date of disclosure of the study information 2010/10/08
Last modified on 2012/10/05 09:44:06

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Basic information

Public title

Quantification of amyloid deposition using positron emission tomography with [C-11]AZD2184

Acronym

Amyloid imaging with [C-11]AZD2184

Scientific Title

Quantification of amyloid deposition using positron emission tomography with [C-11]AZD2184

Scientific Title:Acronym

Amyloid imaging with [C-11]AZD2184

Region

Japan


Condition

Condition

Dementia

Classification by specialty

Neurology Psychiatry Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Development of quantification method for amyloid deposition using positron emission tomography with [C-11]AZD2184

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Distribution volume and binding potential measured by positron emission tomography with [C-11]AZD2184
- Comparison between quantification methods
- Comparison between patients and age- and gender-matched normal controls

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

PET, MRI, Neuropsychological test

Interventions/Control_2

PET, MRI, Neuropsychological test

Interventions/Control_3

PET, MRI, Neuropsychological test

Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

50 years-old <=

Age-upper limit

84 years-old >=

Gender

Male and Female

Key inclusion criteria

Normal controls
- Subjects who have the ability to provide informed consent
- Memory Complaints
None
- Memory Function
Logical Memory II subscale (delayed Paragraph Recall) from the Wechsler Memory Scaled - Revised (the maximum score is 25):
a) more than or equal to 9 for 16 or more years of education
b) more than or equal to 5 for 10-15 years of education
c) more than or equal to 3 for 0-9 years of education
- MMSE
24-30
- CDR
0
Memory Box score must be 0
- General Cognition
Cognitively normal, based on an absence of significant impairment in cognitive functions or activities of daily living
- Hachinski
Modified Hachinski score of less than or equal to 4

Mild cognitive impairment
- Memory Complaints
Memory complaint by subject or study partner that is verified by a study partner
- Memory Function
Logical Memory II subscale (Delayed Paragraph Recall) from the Wechsler Memory Scale - Revised:
a) less than or equal to 8 for 16 or more years of education
b) less than or equal to 4 for 10-15 years of education
c) less than or equal to 2 for 0-9 years of education
- MMSE
24-30
- CDR
0.5
Memory Box score must be at least 0.5
- General Cognition
General cognition and functional performance sufficiently preserved such that a diagnosis of Alzheimer's disease cannot be made by the site physician at the time of the screening visit
- Hachinski
Modified Hachinski score of less than or equal to 4

Alzheimer's disease
- Memory Complaints
Memory complaint by subject or study partner that is verified by a study partner
- Memory Function
(Same as mild cognitive impairment)
- MMSE
12-26
- CDR
0.5-2
- General Cognition
NINCDS/ADRDA criteria for probable AD
- Hachinski
Modified Hachinski score of less than or equal to 4

Key exclusion criteria

Exclusion criteria for patients
- Other psychiatric disorders including drug dependence
- Brain organic diseases including cerebrovascular diseases, Parkinson's disease and other related disorders
- Serious medical illness
- Subjects who are judged as not suitable for participation in this study

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroshi Ito, M.D., Ph.D.

Organization

National Institute of Radiological Sciences

Division name

Molecular Imaging Center

Zip code


Address

4-9-1 Anagawa, Inage-ku, Chiba 263-8555, Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

National Institute of Radiological Sciences

Division name

Molecular Imaging Center

Zip code


Address


TEL


Homepage URL


Email



Sponsor or person

Institute

National Institute of Radiological Sciences

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2010 Year 10 Month 08 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2010 Year 06 Month 16 Day

Date of IRB


Anticipated trial start date

2010 Year 10 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2010 Year 10 Month 05 Day

Last modified on

2012 Year 10 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005184


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name