UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045936
Receipt number R000052437
Scientific Title Japan Neuroimmune Disease Registry
Date of disclosure of the study information 2021/11/20
Last modified on 2024/11/11 12:13:51

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Basic information

Public title

Japan Neuroimmune Disease Registry

Acronym

JANIMA

Scientific Title

Japan Neuroimmune Disease Registry

Scientific Title:Acronym

JANIMA

Region

Japan


Condition

Condition

Neuroimmune Disease

Classification by specialty

Neurology

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

We will clarify the natural history and prognostic factors of neuroimmune diseases by accumulating and reviewing clinical information over a long period of time.

Basic objectives2

Others

Basic objectives -Others

We will establish a system to enable efficient recruitment of patients for clinical trials. This will contribute to the development and establishment of new treatment methods for neuroimmune diseases in the future.

Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

The course of clinical endpoints mainly used for each neuroimmune disease.

Key secondary outcomes

1. EQ-5D-5L
2. Treatment response
3. Frequency of adverse events


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

As follows:
Chronic inflammatory demyelinating polyneuropathy (CIDP)
1) Patients who diagnosed the EFNS/PNS diagnostic criteria 2010 definite, probable, possible
2) Patients who have given written consent to participate in the study
Anti myelin associated glycoprotein (MAG) antibody associated neuropathy
1) Patients with demyelinating polyneuropathy and anti-MAG or anti-SGPG antibody positive.
2) Patients who have given written consent to participate in the study
Multifocal motor neuropathy (MMN)
1) Patients who meet the EFNS/PNS diagnostic criteria 2010 definite, probable, possible
2) Patients who give written consent to participate in the study

Key exclusion criteria

Patients deemed inappropriate for inclusion by the investigator.

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Satoshi
Middle name
Last name Kuwabara

Organization

Graduate School of Medicine and School of Medicine, Chiba University

Division name

Department of Neurology, Professor

Zip code

2608677

Address

1-8-1 Inohana, Chuo-ku, Chiba City, Chiba Prefecture

TEL

0432262126

Email

kuwabara-s@faculty.chiba-u.jp


Public contact

Name of contact person

1st name Shigeki
Middle name
Last name Omori

Organization

General Incorporated Association kizuna

Division name

Secretariat

Zip code

2600856

Address

1-8-15 Inohana, Chuo-ku, Chiba City, Chiba Prefecture

TEL

0432397670

Homepage URL

https://www.janima.org

Email

info@kizuna-cro.org


Sponsor or person

Institute

The Japanese Society for Neuroimmunology

Institute

Department

Personal name



Funding Source

Organization

General Incorporated Association kizuna

Organization

Division

Category of Funding Organization

Other

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

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

2021 Year 11 Month 20 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

2021 Year 08 Month 26 Day

Date of IRB

2021 Year 08 Month 26 Day

Anticipated trial start date

2021 Year 11 Month 20 Day

Last follow-up date

2041 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Although the research period is permanent, ethical review approval and research permission will be obtained every five years.


Management information

Registered date

2021 Year 10 Month 30 Day

Last modified on

2024 Year 11 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052437