UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008018
Receipt number R000009430
Scientific Title Autonomic and Electrocardiographic Tests Study for Diagnosis in Patients with Syncope
Date of disclosure of the study information 2012/06/01
Last modified on 2016/06/23 11:31:08

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Autonomic and Electrocardiographic Tests Study for Diagnosis in Patients with Syncope

Acronym

Autonomic and Electrocardiographic Tests Study for Diagnosis in Patients with Syncope

Scientific Title

Autonomic and Electrocardiographic Tests Study for Diagnosis in Patients with Syncope

Scientific Title:Acronym

Autonomic and Electrocardiographic Tests Study for Diagnosis in Patients with Syncope

Region

Japan


Condition

Condition

Syncope

Classification by specialty

Medicine in general Cardiology Neurology
Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate diagnostic utility and utility of risk-stratification for traffic accident using autonomic and electrocardiographic tests in patients with syncope

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

syncope, presyncope

Key secondary outcomes

arrhythmic events, syncope/presyncope during driving


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

15 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

Study subjects are patients with myocardial infarction, coronary spastic angina, idiopathic cardiomyopathy and pulmonary hypertension, who are stable disease condition, and are suspected as cardiogenic, vasogenic and neurally mediated syncope.

Control subjects are healthy volunteers.

Key exclusion criteria

Exclusion criteria are:
unstable disease condition; other cause of syncope as like traumatic or neurological syncope, or hypoglycemia; patients who do not not accept study enrollment or are difficult to follow-up their clinical course.

Target sample size

250


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yosuke Miwa

Organization

Kyorin University School of Medicine

Division name

Second Department of Internal Medicine

Zip code


Address

6-20-2 Shinkawa, Mitaka. Tokyo, Japan

TEL

+81-422-47-5511

Email

y-miwa@ks.kyorin-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yosuke Miwa

Organization

Arrythmia Center

Division name

Department of Cardiology

Zip code


Address

6-20-2 Shinkawa, Mitaka, Tokyo, Japan

TEL

+81-422-47-5511

Homepage URL


Email

y-miwa@ks.kyorin-u.ac.jp


Sponsor or person

Institute

Second Department of Internal Medicine, Kyorin University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

National Mutual Insurance Federation
of Agricultural Cooperatives

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)

The Promotion of Mutual Aid Corporation for Private Schools of Japan


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

杏林大学医学部附属病院(東京都)


Other administrative information

Date of disclosure of the study information

2012 Year 06 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

Enrolling by invitation

Date of protocol fixation

2012 Year 05 Month 18 Day

Date of IRB


Anticipated trial start date

2012 Year 05 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

Prospective study


Management information

Registered date

2012 Year 05 Month 23 Day

Last modified on

2016 Year 06 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009430


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name