UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017710
Receipt number R000020518
Scientific Title Efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops
Date of disclosure of the study information 2015/07/01
Last modified on 2018/03/24 11:22:45

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Basic information

Public title

Efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops

Acronym

Efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops

Scientific Title

Efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops

Scientific Title:Acronym

Efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops

Region

Japan


Condition

Condition

Meniere's disease, delayed endolymphatic hydrops

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

An attempt was made to examine the efficacy of middle ear pressure therapy in patients with intractable Meniere's disease and delayed endolymphatic hydrops.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Monthly-averaged frequency of vertigo attack

Key secondary outcomes

Vestibular and auditory functions


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

The 3 min-application of positive-negative pressure to the external auditory canal with the middle ear pressure therapy device t.i.d. for 16 weeks.

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

Adult (20-80 y/o) patients with intractable definite Meniere's disease and delayed endolymphatic hydrops

Key exclusion criteria

1) Patients with otitis media.
2) Patients with cardiac pacemaker and implantable cardiac defibrillator.
3) Patients with diseases of the auricle and external auditory canal.
4) Patients who was excluded by investigators.

Target sample size

180


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Noriaki Takeda

Organization

University of Tokushima School of Medicine

Division name

Department of Otolaryngology

Zip code


Address

3-18-15 Kuramoto, Tokushima 770-8503, Japan

TEL

088-633-7169

Email

takeda@tokushima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Noriaki Takeda

Organization

University of Tokushima School of Medicine

Division name

Department of Otolaryngology

Zip code


Address

3-18-15 Kuramoto, Tokushima 770-8503, Japan

TEL

088-633-7169

Homepage URL


Email

takeda@tokushima-u.ac.jp


Sponsor or person

Institute

University of Tokushima

Institute

Department

Personal name



Funding Source

Organization

Grant-in-Aid from the Japan Agency for Medical Research and Development

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 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

Completed

Date of protocol fixation

2015 Year 06 Month 22 Day

Date of IRB


Anticipated trial start date

2015 Year 07 Month 01 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 27 Day

Last modified on

2018 Year 03 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020518


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name