UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017479
Receipt number R000020259
Scientific Title Quantitative assessment of pharyngeal and cervical esophageal pressure with High Resolution Manometry System
Date of disclosure of the study information 2015/05/10
Last modified on 2015/05/09 17:25:11

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Basic information

Public title

Quantitative assessment of pharyngeal and cervical esophageal pressure with High Resolution Manometry System

Acronym

Measurement of pharyngeal and cervical esophageal pressure with High Resolution Manometry System

Scientific Title

Quantitative assessment of pharyngeal and cervical esophageal pressure with High Resolution Manometry System

Scientific Title:Acronym

Measurement of pharyngeal and cervical esophageal pressure with High Resolution Manometry System

Region

Japan


Condition

Condition

dysphagia

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To study each pressure of pharynx and cervical esophagus, quantitatively and objectively with High Resolution Manometry System. Clinically, to evaluate each part of swallowing function in a pharyngeal and esophageal cavity.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Value of swallowing pressure from nasopharynx to cervical esophagus

Key secondary outcomes

Velocity of swallowing
Distal contractile integral in a cavity of oropharynx


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Device, equipment

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

Patients with dysphagia or suspicion of dysphagia
Patients that communication is possible
Patients have adequate function of vital organ
Patients provide written informed consent before initiation of study

Key exclusion criteria

Serious psychiatric disorder
Patients that will be inappropriate for entry into this study in the judgment of the investigator.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kenkichiro Taira

Organization

Tottori University Hospital

Division name

Depertment Otolaryngology:Head and Neck surgery

Zip code


Address

Nishimachi 36-1, Yonago, Tottori, Japan

TEL

0859-38-6627

Email

kenkitiroutairaarea@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kenkichiro Taira

Organization

Tottori University Hospital

Division name

Depertment Otolaryngology:Head and Neck surgery

Zip code


Address

Nishimachi 36-1, Yonago, Tottori, Japan

TEL

0859-38-6627

Homepage URL


Email

kenkitiroutairaarea@yahoo.co.jp


Sponsor or person

Institute

Tottori University Hospital

Institute

Department

Personal name



Funding Source

Organization

Tottori University Hospital

Organization

Division

Category of Funding Organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2015 Year 05 Month 10 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

Preinitiation

Date of protocol fixation

2015 Year 04 Month 01 Day

Date of IRB


Anticipated trial start date

2015 Year 05 Month 10 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 05 Month 09 Day

Last modified on

2015 Year 05 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020259


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name