UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045381
Receipt number R000051822
Scientific Title Investigation of cough function in patients with multiple system atrophy
Date of disclosure of the study information 2021/09/06
Last modified on 2024/03/18 09:04:50

* 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

Investigation of cough function in patients with multiple system atrophy

Acronym

Investigation of cough function in patients with multiple system atrophy

Scientific Title

Investigation of cough function in patients with multiple system atrophy

Scientific Title:Acronym

Investigation of cough function in patients with multiple system atrophy

Region

Japan


Condition

Condition

Multiple system atrophy

Classification by specialty

Neurology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Investigate how cough function in patients with multiple system atrophy changes as the stage progresses

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Peak cough flow

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

30 years-old <=

Age-upper limit

100 years-old >

Gender

Male and Female

Key inclusion criteria

Patients diagnosed with probable MSA according to the MSA international consensus criteria (Gilman's diagnostic / classification criteria).

Key exclusion criteria

1:Respiratory disease
2:Heart disease
3:Neoplastic disease
4:Patients with other neurological disorders or neuromuscular disorders
5:Acute or chronic inflammatory and infectious diseases
6:Patients who have undergone tracheostomy or are using artificial respiration therapy under tracheostomy
7:Patients who cannot communicate at all due to severe dementia
8:Patients who cannot communicate at all due to communication disorders

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Takashi
Middle name
Last name Asakawa

Organization

International university of health and welfare graduate school of medicine,Department of Clinical Medical Sciences,Rehabilitation Medicine

Division name

Department of rehabilitation

Zip code

272-0827

Address

6-1-14, Konodai, Ichikawa city, Chiba prefecture, Japan

TEL

047-375-1111

Email

takashi.rpt@gmail.com


Public contact

Name of contact person

1st name Takashi
Middle name
Last name Asakawa

Organization

International university of health and welfare ICHIKAWA hospital

Division name

Department of rehabilitation

Zip code

272-0827

Address

6-1-14, Konodai, Ichikawa city, Chiba prefecture, Japan

TEL

047-375-1111

Homepage URL


Email

takashi.rpt@gmail.com


Sponsor or person

Institute

International university of health and welfare

Institute

Department

Personal name



Funding Source

Organization

None

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

International University of Health and Welfare Chiba District Ethics Review Board

Address

4-3, Kozunomori, Narita city, Chiba prefecture, Japan

Tel

0476-20-7708

Email

rinri_md@iuhw.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 09 Month 06 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

Main results already published

Date of protocol fixation

2021 Year 06 Month 22 Day

Date of IRB

2021 Year 06 Month 22 Day

Anticipated trial start date

2021 Year 06 Month 22 Day

Last follow-up date

2023 Year 01 Month 31 Day

Date of closure to data entry

2023 Year 01 Month 31 Day

Date trial data considered complete

2023 Year 02 Month 01 Day

Date analysis concluded

2023 Year 02 Month 15 Day


Other

Other related information

Cross-sectional assessment of cough function in patients with multiple system atrophy


Management information

Registered date

2021 Year 09 Month 05 Day

Last modified on

2024 Year 03 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051822


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name