UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000032429
Receipt number R000036982
Scientific Title Simple recording of eye movement at home
Date of disclosure of the study information 2018/04/30
Last modified on 2019/05/01 16:01:41

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Basic information

Public title

Simple recording of eye movement at home

Acronym

Simple recording of eye movement at home

Scientific Title

Simple recording of eye movement at home

Scientific Title:Acronym

Simple recording of eye movement at home

Region

Japan


Condition

Condition

Diseases causing paroxysmal vertigo attack

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To use the eye movement recording system to patients with paroxysmal vertigo attack for the diagnosis.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Recorded movie of eye movement

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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Device for recording eye movement

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

2 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

# Patients who complain vertigo attack and are more than 2 years old.
# Patients who assent this study and can use the device of this study at home.

Key exclusion criteria

# Patients who do not assent this study.
# Patients who can not use the device of this study at home.
# Patients whose contact information is unclear.
# Patients who are judged to be unsuitable to this study by doctors.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name TAKAO
Middle name
Last name IMAI

Organization

Osaka University

Division name

Otolaryngology, Head & Neck Surgery

Zip code

565-0871

Address

2-2 Yamadaoka, Suita, Osaka 565-0871 Japan

TEL

06-6879-3951

Email

timai@ent.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name Takao
Middle name
Last name IMAI

Organization

Osaka University Hospital

Division name

Otolaryngology, Head and Neck Surgery

Zip code

565-0871

Address

2-2 Yamadaoka, Suita, Osaka 565-0871 Japan

TEL

06-6879-5575

Homepage URL


Email

timai@ent.med.osaka-u.ac.jp


Sponsor or person

Institute

Osaka University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Osaka University Graduate School of Medicine

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

Osaka University

Address

2-2 Yamadaoka, Suita, Osaka 565-0871 Japan

Tel

06-6879-5111

Email

rinri@hp-crc.med.osaka-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



Other administrative information

Date of disclosure of the study information

2018 Year 04 Month 30 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

2013 Year 11 Month 14 Day

Date of IRB

2013 Year 11 Month 14 Day

Anticipated trial start date

2013 Year 12 Month 01 Day

Last follow-up date

2023 Year 12 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

2018 Year 04 Month 30 Day

Last modified on

2019 Year 05 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000036982


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name