UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022849
Receipt number R000026333
Scientific Title Evaluation study of serotonin 1B receptors in mental disorders by positron emission tomography
Date of disclosure of the study information 2016/06/27
Last modified on 2022/12/28 13:37:14

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Evaluation study of serotonin 1B receptors in mental disorders by positron emission tomography

Acronym

Evaluation study of serotonin 1B receptors in mental disorders

Scientific Title

Evaluation study of serotonin 1B receptors in mental disorders by positron emission tomography

Scientific Title:Acronym

Evaluation study of serotonin 1B receptors in mental disorders

Region

Japan


Condition

Condition

Organic and symptomatic mental disorders, Schizophrenia, mood disorders, anxiety disorders, nonorganic insomnia

Classification by specialty

Psychiatry Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the serotonin 1B receptors of mental disorders

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

evaluation of the serotonin 1B receptor of mental disorders by PET

Key secondary outcomes

cognitive function by neuropsychological test, MRI, blood concentration, sleep state


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

PET ([11C]AZ20149369 370MBq), MRI, blood concentration

Interventions/Control_2


Interventions/Control_3


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

20 years-old <=

Age-upper limit

80 years-old >

Gender

Male and Female

Key inclusion criteria

- Patients who diagnosed as F0, F2, F3, F4, F5 by ICD-10
- healthy control

Key exclusion criteria

- with past or current history of serious medical illness and/or brain organic diseases
- subject who is contraindicated for the use of MRI
- with past or current history ofsevere liver disease, kidney disease, heart disease, allergy, or severe drug allergy
- pregnant woman
- subject who are judged as not suitable for participation in this study

Target sample size

80


Research contact person

Name of lead principal investigator

1st name Yoshiro
Middle name
Last name Okubo

Organization

Nippon Medical School

Division name

Department of Neuropsychiatry

Zip code

113-8602

Address

1-1-5 Sendagi, Bunkyo-ku, Tokyo, Japan

TEL

+81-3-3822-2131

Email

okubo-y@nms.ac.jp


Public contact

Name of contact person

1st name Amane
Middle name
Last name Tateno

Organization

Nippon Medical School

Division name

Department of Neuropsychiatry

Zip code

113-8602

Address

1-1-5 Sendagi, Bunkyo-ku , Tokyo, Japan

TEL

+81-3-3822-2131

Homepage URL


Email

amtateno@nms.ac.jp


Sponsor or person

Institute

Nippon Medical School

Institute

Department

Personal name



Funding Source

Organization

MEXT

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nippon Medical School Hospital Institutional Review Board

Address

1-1-5, Sendagi, Bunkyo-ku, Tokyo, Japan

Tel

+81-3-3822-2131

Email

clinicaltrial@nms.ac.jp


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

2016 Year 06 Month 27 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

No longer recruiting

Date of protocol fixation

2016 Year 05 Month 31 Day

Date of IRB

2016 Year 05 Month 20 Day

Anticipated trial start date

2016 Year 06 Month 30 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry

2019 Year 06 Month 30 Day

Date trial data considered complete

2019 Year 09 Month 30 Day

Date analysis concluded

2023 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2016 Year 06 Month 23 Day

Last modified on

2022 Year 12 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026333


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name