UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020762
Receipt number R000023964
Scientific Title Assessment of the atrial fibrillation ablation outcome
Date of disclosure of the study information 2016/04/01
Last modified on 2017/03/03 18:14:46

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Basic information

Public title

Assessment of the atrial fibrillation ablation outcome

Acronym

Assessment of the atrial fibrillation ablation outcome

Scientific Title

Assessment of the atrial fibrillation ablation outcome

Scientific Title:Acronym

Assessment of the atrial fibrillation ablation outcome

Region

Japan


Condition

Condition

atrial fibrillation

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The outcome of atrial fibrillation catheter ablation was assessed by utilizing 24-hour Holter ECG and telemonitoring ECG.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Relapse of atrial fibrillation after catheter ablation
The post operative 6-month monitoring using Holter ECG and telemonitoring ECG

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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

monthly Holter ECG, telemonitoring ECG twice daily
During the postoperative 6 months

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


Not applicable

Age-upper limit

75 years-old >

Gender

Male and Female

Key inclusion criteria

Candidates for catheter ablation of atrial fibrillation

Key exclusion criteria

Contraindiation for catheter ablation of atrial fibrillation

Target sample size

31


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Seiji Takatsuki

Organization

Keio University School of Medicine

Division name

Department of Cardiology

Zip code


Address

35 Shinanomachi Shinjuku-ku

TEL

0333531211

Email

seiji.takatsuki@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Takehiro Kimura

Organization

Keio University School of Medicine

Division name

Department of Cardiology

Zip code


Address

35 Shinanomachi Shinjuku-ku

TEL

0333531211

Homepage URL


Email

kimura@z7.keio.jp


Sponsor or person

Institute

Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Keio University 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


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

2016 Year 04 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

http://www.ncbi.nlm.nih.gov/pubmed/27385021

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

Main results already published

Date of protocol fixation

2013 Year 06 Month 24 Day

Date of IRB


Anticipated trial start date

2013 Year 07 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



Management information

Registered date

2016 Year 01 Month 27 Day

Last modified on

2017 Year 03 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023964


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name