UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008943
Receipt number R000010486
Scientific Title Prospective Randomized Controlled Study for Clinical Application of the Hanger Reflex to Treat Cervical Dystonia
Date of disclosure of the study information 2012/09/24
Last modified on 2021/10/01 15:32:42

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Basic information

Public title

Prospective Randomized Controlled Study for Clinical Application of the Hanger Reflex to Treat Cervical Dystonia

Acronym

RCT Study for Hanger Reflex

Scientific Title

Prospective Randomized Controlled Study for Clinical Application of the Hanger Reflex to Treat Cervical Dystonia

Scientific Title:Acronym

RCT Study for Hanger Reflex

Region

Japan


Condition

Condition

Cevical dystonia

Classification by specialty

Neurology Neurosurgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess a portable device which induces the hanger reflex and to evaluate the efficacy of it for the cervical dystonia patients.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Toronto Western Spasmodic Torticollis Rating Scale and modified Tsui score

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Put the device on the subject's head by proper way for 10 minutes during the study.

Interventions/Control_2

Put the device on the subject's head by ineffective way for 10 minutes during the study.

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with mainly rotational cervical dystonia.

Key exclusion criteria

1. Unstable symptom
2. Patients who cannnot understand the purpose of the study
3. Patients who are deemed to be disqualified by PI or co-investigator.

Target sample size

70


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Genko Oyama

Organization

Juntendo University

Division name

Department of Neurology

Zip code


Address

2-1-1 Hongo, Bunkyo, Tokyo

TEL

+81-3-3813-3111

Email



Public contact

Name of contact person

1st name
Middle name
Last name Genko Oyama

Organization

Juntendo University

Division name

Department of Neurology

Zip code


Address

2-1-1 Hongo, Bunkyo, Tokyo

TEL

+81-3-3813-3111

Homepage URL


Email

g_oyama@juntendo.ac.jp


Sponsor or person

Institute

Juntendo University, Department of Neurology

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

Japan


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

2012 Year 09 Month 24 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

Terminated

Date of protocol fixation

2012 Year 09 Month 24 Day

Date of IRB

2012 Year 09 Month 12 Day

Anticipated trial start date

2012 Year 09 Month 24 Day

Last follow-up date

2014 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

2012 Year 09 Month 19 Day

Last modified on

2021 Year 10 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010486


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name