UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043156
Receipt number R000049264
Scientific Title Examination of changes of water amount in the pharyngeal cavity with the head and neck flexion position using a new swallowing evaluation method
Date of disclosure of the study information 2022/08/08
Last modified on 2023/08/05 12:57:58

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Basic information

Public title

Examination of changes of water amount in the pharyngeal cavity with the head and neck flexion position using a new swallowing evaluation method

Acronym

Examination of changes of water amount in the pharyngeal cavity with the head and neck flexion position using a new swallowing evaluation method

Scientific Title

Examination of changes of water amount in the pharyngeal cavity with the head and neck flexion position using a new swallowing evaluation method

Scientific Title:Acronym

Examination of changes of water amount in the pharyngeal cavity with the head and neck flexion position using a new swallowing evaluation method

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Using a new swallowing evaluation method, we observe swallowing dynamics in the head flexion position, neck flexion position, head and neck flexion position, and neutral posture.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Observation of swallowing dynamics in head flexion position, neck flexion position, head and neck flexion position, and neutral position

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Ingestion of contrast medium

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

65 years-old >=

Gender

Male and Female

Key inclusion criteria

Healthy person
Those who have no problem with swallowing evaluation screening

Key exclusion criteria

Iodine allergy

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Nobuyuki
Middle name
Last name Arai

Organization

Kawasaki Medical School

Division name

Department of Rehabilitation Medicine

Zip code

701-0192

Address

577 Matsushima, Kurashiki-shi, Okayama

TEL

086-462-1111

Email

dodobiyan@med.kawasaki-m.ac.jp


Public contact

Name of contact person

1st name Nobuyuki
Middle name
Last name Arai

Organization

Kawasaki Medical School

Division name

Department of Rehabilitation Medicine

Zip code

701-0192

Address

577 Matsushima, Kurashiki-shi, Okayama

TEL

086-462-1111

Homepage URL


Email

dodobiyan@med.kawasaki-m.ac.jp


Sponsor or person

Institute

Kawasaki Medical School

Institute

Department

Personal name



Funding Source

Organization

Self funding

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kawasaki Medical School / Hospital Ethics Committee

Address

577 Matsushima, Kurashiki-shi, Okayama

Tel

086-462-1111

Email

kmsrec@med.kawasaki-m.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

2022 Year 08 Month 08 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 01 Month 27 Day

Date of IRB

2021 Year 01 Month 27 Day

Anticipated trial start date

2021 Year 04 Month 01 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 01 Month 27 Day

Last modified on

2023 Year 08 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049264


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name