UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000050210
Receipt number R000056016
Scientific Title Fundamental survey registry research in the field of neurodegenerative diseases
Date of disclosure of the study information 2023/02/01
Last modified on 2023/02/01 14:19:29

* 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

Fundamental survey registry research in the field of neurodegenerative diseases

Acronym

Fundamental survey registry research in the field of neurodegenerative diseases

Scientific Title

Fundamental survey registry research in the field of neurodegenerative diseases

Scientific Title:Acronym

Fundamental survey registry research in the field of neurodegenerative diseases

Region

Japan


Condition

Condition

neurodegenerative diseases

Classification by specialty

Neurology Pediatrics Psychiatry
Neurosurgery Adult Child

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We will accumulate clinical information of patients in the area of neurodegenerative diseases and examine the evaluation items continuously and long-term.

Basic objectives2

Others

Basic objectives -Others

We will elucidate the natural history and prognostic factors of neurodegenerative diseases, and contribute to the development and establishment of new treatments for neurodegenerative diseases in the future.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The goal is to establish a continuous case accumulation system for patients with neurodegenerative diseases.

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1)Patients who have been diagnosed with possible disease according to each diagnostic criteria in the area of neurodegenerative diseases
2)Patients who gave written informed consent to participate in the study

Key exclusion criteria

1) Patients who are judged to be inappropriate as subjects by the judgment of researchers, etc.

Target sample size

99999


Research contact person

Name of lead principal investigator

1st name Hisanori
Middle name
Last name Kowa

Organization

National Hospital Organization Matsue Medical Center

Division name

Honorary Director

Zip code

690-8556

Address

5-8-31 Agenogi, Matsue-city, Shimane Pref., JAPAN

TEL

0852-21-6131

Email

nakashima.kenji.np@mail.hosp.go.jp


Public contact

Name of contact person

1st name Hisanori
Middle name
Last name Kowa

Organization

National Hospital Organization Matsue Medical Center

Division name

Deputy Director

Zip code

690-8556

Address

5-8-31 Agenogi, Matsue-city, Shimane Pref., JAPAN

TEL

0852-21--6131

Homepage URL


Email

norkowa-neu@umin.ac.jp


Sponsor or person

Institute

the Ministry of Health, Labour and Welfare

Institute

Department

Personal name



Funding Source

Organization

the Ministry of Health, Labour and Welfare

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

Kyoto University Graduate School and Faculty of Medicine, Ethics Committee

Address

Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, JAPAN

Tel

075-753-4680

Email

ethcom@kuhp.kyoto-u.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

2023 Year 02 Month 01 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

Open public recruiting

Date of protocol fixation

2022 Year 04 Month 15 Day

Date of IRB

2022 Year 04 Month 20 Day

Anticipated trial start date

2022 Year 05 Month 01 Day

Last follow-up date

2025 Year 04 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This work has been supported by Grants-in Aid from the Research Committee of CNS Degenerative Diseases, Research on Policy Planning and Evaluation for Rare and Intractable Diseases, Health, Labour and Welfare Sciences Research Grants, the Ministry of Health, Labour and Welfare, Japan


Management information

Registered date

2023 Year 02 Month 01 Day

Last modified on

2023 Year 02 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056016


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name