UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056606
Receipt number R000064689
Scientific Title Proof that a maneuver to restore positional nystagmus from benign paroxysmal positional vertigo fatigue in patients with bilateral posterior canal type of benign paroxysmal positional vertigo selectively restores positional nystagmus only on the side where the maneuver was performed - a crossover study
Date of disclosure of the study information 2025/01/06
Last modified on 2025/07/01 12:19:15

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Basic information

Public title

Proof that a maneuver to restore positional nystagmus from benign paroxysmal positional vertigo fatigue in patients with bilateral posterior canal type of benign paroxysmal positional vertigo selectively restores positional nystagmus only on the side where the maneuver was performed - a crossover study

Acronym

Efficacy of a maneuver to restore positional nystagmus from BPPV fatigue in patients with bilateral posterior canal type of BPPV

Scientific Title

Proof that a maneuver to restore positional nystagmus from benign paroxysmal positional vertigo fatigue in patients with bilateral posterior canal type of benign paroxysmal positional vertigo selectively restores positional nystagmus only on the side where the maneuver was performed - a crossover study

Scientific Title:Acronym

Efficacy of a maneuver to restore positional nystagmus from BPPV fatigue in patients with bilateral posterior canal type of BPPV

Region

Japan


Condition

Condition

Bilateral posterior canals type of benign paroxysmal positional vertigo

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to demonstrate that a maneuver for restoring positional nystagmus that has disappeared due to benign paroxysmal positional vertigo fatigue in patients with bilateral posterior canals type of benign paroxysmal positional vertigo restores only positional nystagmus on the side on which the maneuver is performed, and does not restore positional nystagmus on the other side, in other words, that this maneuver has a selective effect on the side on which the maneuver is performed.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Maximum slow phase eye velocity of positional nystagmus after a maneuver to restore positional nystagmus from benign paroxysmal positional vertigo fatigue

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

A maneuver is performed to restore positional nystagmus caused by benign paroxysmal positional vertigo fatigue.

Interventions/Control_2

A maneuver is not performed to restore positional nystagmus caused by benign paroxysmal positional vertigo fatigue.

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

Outpatients (20-95 years old) at our hospital whose complaint was dizziness and/or vertigo and whose B score was 2 or more than 2.

Key exclusion criteria

Patients who do not consent to participate, have a medical history or possibility of cervical or lumber disease, have severe heart disease, or are possibly pregnant, and pregnant women.

Target sample size

15


Research contact person

Name of lead principal investigator

1st name Ta
Middle name
Last name Imai

Organization

Bell Land General Hospital

Division name

Otorhinolaryngology - Head and Neck Surgery

Zip code

599-8247

Address

500-3, Higashi-yama, Naka-ku, Sakai-shi, Osaka, Japan

TEL

0722342001

Email

imaitakao@hotmail.com


Public contact

Name of contact person

1st name Sayaka
Middle name
Last name Yasuda

Organization

Bell Land General Hospital

Division name

Clinical Research Review Board

Zip code

599-8247

Address

500-3 Higashi-yama, Naka-ku, Sakai-shi, Osaka, Japan

TEL

0722342001

Homepage URL


Email

irb@bh.seichokai.or.jp


Sponsor or person

Institute

Department of Otorhinolaryngology - Head and Neck Surgery, Bell Land General Hospital Takao Imai

Institute

Department

Personal name



Funding Source

Organization

JSPS KAKENHI grant

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Bell Land General Hospital

Address

500-3 Higashi-yama, Naka-ku, Sakai-shi, Osaka, Japan

Tel

0722342001

Email

irb@bh.seichokai.or.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

2025 Year 01 Month 06 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

2024 Year 12 Month 27 Day

Date of IRB

2024 Year 12 Month 27 Day

Anticipated trial start date

2025 Year 01 Month 06 Day

Last follow-up date

2025 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

2024 Year 12 Month 30 Day

Last modified on

2025 Year 07 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064689