UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027661
Receipt number R000027789
Scientific Title Sutudy of the Swallowing Sounds Recorded through the Ear
Date of disclosure of the study information 2017/07/01
Last modified on 2023/11/14 09:56:07

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Basic information

Public title

Sutudy of the Swallowing Sounds Recorded through the Ear

Acronym

Swallowing Sounds Recorded through the Ear

Scientific Title

Sutudy of the Swallowing Sounds Recorded through the Ear

Scientific Title:Acronym

Swallowing Sounds Recorded through the Ear

Region

Japan


Condition

Condition

Dysphagia

Classification by specialty

Oto-rhino-laryngology Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine whether intra-aural swallowing sounds can be clinically applied as a temporal indicator of swallowing function.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Time of intra-aural swallowing sounds

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

20 years-old <=

Age-upper limit

95 years-old >=

Gender

Male and Female

Key inclusion criteria

1.There is a difficulty swallowing feeling
2.20 years of age or older men and women
3.Written consent was obtained
4.Otolaryngologist has determined that there is no ear disease

Key exclusion criteria

1.Minor
2.Have inserted a tracheotomy cannula
3.Have inserted a stomach tube
4.Suspected inflammatory condition
5.It is inhaled continuously oxygen
During pregnancy

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Takashi
Middle name
Last name Nakagawa

Organization

Graduate School of Medical Sciences, Kyushu University

Division name

Department of Otorhinolaryngology

Zip code

812-8582

Address

3-1-1Maidashi Higashi-ku Fukuoka

TEL

092-642-5668

Email

styama@qent.med.kyushu-u.ac.jp


Public contact

Name of contact person

1st name Yumi
Middle name
Last name Yamaguchi

Organization

Graduate School of Medical Sciences, Kyushu University

Division name

Department of Otorhinolaryngology

Zip code

812-8582

Address

3-1-1Maidashi Higashi-ku Fukuoka

TEL

092-642-5668

Homepage URL


Email

styama@qent.med.kyushu-u.ac.jp


Sponsor or person

Institute

Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University.

Institute

Department

Personal name



Funding Source

Organization

Grant-in-Aid for Scientific Research

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

Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University.

Address

3-1-1 Maidashi Higashi-ku Fukuoka 812-8582 Japan

Tel

092-642-5668

Email

styama@qent.med.kyushu-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

九州大学病院


Other administrative information

Date of disclosure of the study information

2017 Year 07 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

Enrolling by invitation

Date of protocol fixation

2017 Year 06 Month 09 Day

Date of IRB

2017 Year 06 Month 09 Day

Anticipated trial start date

2017 Year 06 Month 09 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

no


Management information

Registered date

2017 Year 06 Month 06 Day

Last modified on

2023 Year 11 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027789


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name