UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019459
Receipt number R000019809
Scientific Title Assess the EFfects of RAte ReSponse AlgoriThm on the prEvention of AtRial Fibrillation
Date of disclosure of the study information 2015/10/22
Last modified on 2015/10/23 14:10:34

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Basic information

Public title

Assess the EFfects of RAte ReSponse AlgoriThm on the prEvention of AtRial Fibrillation

Acronym

FASTER Study

Scientific Title

Assess the EFfects of RAte ReSponse AlgoriThm on the prEvention of AtRial Fibrillation

Scientific Title:Acronym

FASTER Study

Region

Japan


Condition

Condition

Sick sinus syndrome

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess the effcts of rate response algorithm on AF burden in pacemaker patients with sick sinus syndrome

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Total AF burden during 6 months

Key secondary outcomes

Changes of total AF burden, a day averaged AF burden and (atrial- and ventricular)pacing ratio


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

No treatment

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

Rate Response ON during first 6 months
Rate Response OFF during next 6 months

Interventions/Control_2

Rate Response OFF during first 6 months
Rate Response ON during next 6 months

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


Not applicable

Gender

Male and Female

Key inclusion criteria

dual chamber pacemaker patients with sick sinus syndrome

more than 20 years old

willing and capble of providing informed consent

Key exclusion criteria

central nerve system, liver and /or kidny diseases

chronic AF

Complete and advanced AV block


surgical and/or catheter ablation within recent 3 months

pregnancy or plan to become pregnant

all patient who are inappropreate for this study

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masahiro Ogawa

Organization

Fukuoka University School of Medicine

Division name

Department of Cardiology

Zip code


Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka

TEL

092-801-1011

Email

ogawam@adm.fukuoka-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kaoru Hosoi Kaori Urabe

Organization

Fukuoka University School of Medicine

Division name

Department of Cardiology

Zip code


Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka

TEL

092-801-1011

Homepage URL


Email

junkan3@minf.med.fukuoka-u.ac.jp


Sponsor or person

Institute

Department of CardiologyFukuoka University School of medicine

Institute

Department

Personal name



Funding Source

Organization

NPO Clinical and Applied Science, Fukuoka

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor

Yamaguchi University Hospital
Kameda Medical Center
Yokohama Rosai Hospital
Tokuyama Chuo Hospital
Fukuseikai Hospital
Makiyama Chuo Hospital

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

福岡大学病院 Fukuoka University Hospital


Other administrative information

Date of disclosure of the study information

2015 Year 10 Month 22 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

2015 Year 03 Month 18 Day

Date of IRB


Anticipated trial start date

2015 Year 04 Month 09 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 10 Month 22 Day

Last modified on

2015 Year 10 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019809


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name