UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018468
Receipt number R000020233
Scientific Title Japanese Longitudinal Biomarker Study in PSP and CBD
Date of disclosure of the study information 2015/08/01
Last modified on 2021/01/31 14:24:15

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Basic information

Public title

Japanese Longitudinal Biomarker Study in PSP and CBD

Acronym

Japanese Longitudinal Biomarker Study in PSP and CBD (JALPAC)

Scientific Title

Japanese Longitudinal Biomarker Study in PSP and CBD

Scientific Title:Acronym

Japanese Longitudinal Biomarker Study in PSP and CBD (JALPAC)

Region

Japan


Condition

Condition

progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), corticobasal syndrome (CBS)

Classification by specialty

Neurology Geriatrics Psychiatry
Laboratory medicine Adult

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

The present project is a longitudinal observation study. The aims of the study are as follows. 1) To clarify natural history of patients with PSP/CBD syndrome, 2) To explore diagnostic and prognostic biomarker

Basic objectives2

Others

Basic objectives -Others

Validation of published diagnostic criteria for Japanese patients with PSP/CBS

Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

- Elucidation of the natural history
- Development of new biomarker(s)

Key secondary outcomes

- Clinical evaluations including cognitive, language, oculomotor, and motor functions during the observation period.
- Clinical severity
- MRI (volumetric analysis)
- Known CSF and blood biomarkers
- Neuropathological examination


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) Patients 20 years of age or older who provide written informed consent

2) Healthy volunteers 20 years of age or older who provide written informed consent

3) Patients meeting the NINDS-SPSP diagnostic criteria (Litvan 1996)

4) Patients meeting the modified version of the Cambridge CBS diagnostic criteria (Mathew 2012)

5) Patients meeting the CBD diagnostic criteria (Armstrong 2013)

6) Patients who do not meet the diagnostic criteria of PSP/CBS, but clinically suspected as having these conditions

Key exclusion criteria

fulfill the diagnostic criteria of other neurodegenerative disorders

Target sample size

150


Research contact person

Name of lead principal investigator

1st name Takeshi
Middle name
Last name Ikeuchi

Organization

Niigata University, Brain Research Institute

Division name

Center for Bioresource

Zip code

951858

Address

1-757 Asahimachi, Niigata 951-8585, Japan

TEL

025-227-2344

Email

ikeuchi@bri.niigata-u.ac.jp


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Ikeuchi

Organization

Niigata University, Brain Research Institute

Division name

Molecular Genetics

Zip code

951-8585

Address

1-757 Asahimachi, Niigata 951-8585, Japan

TEL

025-227-2344

Homepage URL


Email

ikeuchi@bri.niigata-u.ac.jp


Sponsor or person

Institute

Niigata University, Brain Research Institute

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Research Committee of CNS Degenerative Diseases

Name of secondary funder(s)

MHLW (Japan)


IRB Contact (For public release)

Organization

Research Ethics Committee

Address

1-754 Asahimachi, Niigata 951-8585, Niigata

Tel

025-227-2625

Email

sanonao@adm.niigata-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

鳥取大学病院(鳥取県)/ Tottori University (Tottori),新潟大学医歯学総合病院(新潟県)/ Niigata University (Niigata),神戸大学病院(兵庫県)/ Kobe University (Hyogo),名古屋大学病院(愛知県)/ Nagoya University (Aichi),東京都立神経病院(東京都)/ Tokyo Metropolitan Neurological Hospital (Tokyo),自治医科大学病院(栃木県)/ Jichi Medical University (Tochigi),高知大学(高知県)/ Kochi University (Kochi),松江医療センター(島根県)/ Matsue Medical Center (Shimane),東名古屋病院(愛知県)/ East Nagoya National Hospital (Aichi),倉敷平成病院(岡山県)/ Kurashiki-Heisei Hospital (Okayama),三朝温泉病院(鳥取県)/ Misasa-Onsen Hospital (Tottori),群馬大学病院(群馬県)/ Gunma University (Gunma),京都府立医科大学病院(京都府)/ Kyoto Prefectural University of Medicine,東京都健康長寿医療センター病院(東京都)/ Tokyo Metropolitan Geriatric Hospital (Tokyo),相模原病院(神奈川県)/ Sagamihara National Hospital (Kanagawa),千葉東病院(千葉県)/ Chiba East National Hospital (Chiba),岡山旭東病院(岡山県)/ Okayama Kyokuto Hospital (Okayama),山梨大学(山梨県)/ Yamanashi University (Yamanashi),国立精神・神経研究センター(東京都)/ National Center Hospital NCNP (Tokyo),順天堂大学病院(東京都)/ Juntendo University (Tokyo),愛知医科大学病院(愛知県)/ Aichi Medical University (Aichi),徳島大学(徳島県)/ Tokushima University (Tokushima),ビハーラ花の里病院(広島県)/ Vihara Hananosato Hospital (Hiroshima),東京大学病院(東京都)/ University of Tokyo (Tokyo),老年病研究所病院(群馬県)/ Geriatric Disease Research Hospital (Gunma),三重大学病院(三重県)/ Mie University (Mie),千葉大学病院(千葉県)/ Chiba University (Chiba),順天堂大学越谷病院(埼玉県)/ Juntendo University Koshigaya Hospital (Saitama),東北大学病院(宮城県)/ Tohoku University (Miyagi),岡山大学病院(岡山県)/ Okayama University (Okayama),福岡大学病院(福岡県)/ Fukuoka University (Fukuoka),大阪大学病院(大阪府)/ Osaka University (Osaka),北海道大学病院(北海道)/ Hokkaido University,産業医科大学病院(福岡県)/ University of Occupational and Environmental Health (Fukuoka) / 東京医科歯科大学病院(東京)/ Tokyo Medical and Dental University,国立病院機構 兵庫中央病院 / Hyogo Central Hospital,東邦大学医療センター大森病院 / Toho University Medical Center Ohmori Hospital,国立病院機構 三重病院 / Mie Hospital,富士見高原病院 / Fujimi-Kogen Hospital,群馬大学 / Gunma University Hospital,岐阜大学 / Gifu University Hospital,国立病院機構 鈴鹿病院 / Suzuka Hospital,国立病院機構 新潟病院 / Niigata Hospital,山形大学 / Yamagata University Hospital,桑名総合医療センター / Kuwana General Medical Center,東邦大学医療センター佐倉病院 / Toho University Medical Center Sakura Hospital,福祉村病院 / Fukushimura Hospital


Other administrative information

Date of disclosure of the study information

2015 Year 08 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

2014 Year 11 Month 01 Day

Date of IRB

2014 Year 11 Month 01 Day

Anticipated trial start date

2014 Year 11 Month 17 Day

Last follow-up date

2024 Year 10 Month 15 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This study is a multicenter observational study in which case and control subjects will be recruited and longitudinally followed.


Management information

Registered date

2015 Year 07 Month 29 Day

Last modified on

2021 Year 01 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020233


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name