UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000061664
Receipt number R000068703
Scientific Title ENtire ABLation rEgistry of Osaka CardioVascular Conference: ENABLE-OCVC
Date of disclosure of the study information 2026/05/25
Last modified on 2026/05/22 17:45:29

* 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

ENtire ABLation rEgistry of Osaka CardioVascular Conference: ENABLE-OCVC

Acronym

ENABLE-OCVC registry

Scientific Title

ENtire ABLation rEgistry of Osaka CardioVascular Conference: ENABLE-OCVC

Scientific Title:Acronym

ENABLE-OCVC registry

Region

Japan


Condition

Condition

Arrhythmia

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Catheter ablation (CA), which has become indispensable as a therapeutic option for cardiac arrhythmias, continues to evolve in response to advances in adjunctive technologies and progress in understanding arrhythmia pathophysiology. We will establish a large-scale, multicenter database to continuously update and refine optimal treatment strategies.

Using long-term, large-scale multicenter data, we will comprehensively analyze patient characteristics, indices for pathophysiological assessment, and prognostic information to:

1. continuously pursue optimal treatment strategies;

2. examine the relationships between patient factors, ablation outcomes, and prognosis; and

3. collect clinical data to facilitate the societal implementation of medical informatics and artificial intelligence technologies.

Through these multifaceted, long-term investigations, we aim to generate insights that will contribute to earlier diagnosis and detection and to improved prognosis for patients.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Recurrence within 3 years after catheter ablation

Key secondary outcomes



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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

All patients who underwent catheter ablation at the participating institutions

Key exclusion criteria

Patients who decline participation in the study (opt out).

Patients deemed unsuitable for inclusion by the principal investigator or co-investigators for any reason.

Target sample size

8000


Research contact person

Name of lead principal investigator

1st name Yasushi
Middle name
Last name Sakata

Organization

The University of Osaka Graduate School of Medicine

Division name

Department of Cardiovascular Medicine

Zip code

565-0871

Address

2-2 Yamadaoka, Suita, Osaka

TEL

06-6879-3631

Email

yasushisk@cardiology.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name Yohei
Middle name
Last name Sotomi

Organization

The University of Osaka Graduate School of Medicine

Division name

Department of Cardiovascular Medicine

Zip code

565-0871

Address

2-2 Yamadaoka, Suita, Osaka

TEL

06-6879-3631

Homepage URL


Email

ocvc.hf@gmail.com


Sponsor or person

Institute

The university of Osaka

Institute

Department

Personal name



Funding Source

Organization

The university of Osaka

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

The University of Osaka Hospital Ethical Review Board

Address

2-2 Yamadaoka, Suita, Osaka

Tel

06-6879-5111

Email

rinri@hp-crc.med.osaka-u.ac.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

大阪府


Institutions

Institutions

大阪大学医学部附属病院、独立行政法人 労働者健康安全機構 大阪ろうさい病院、地方独立行政法人 市立東大阪医療センター、社会医療法人 大阪国際メディカル&サイエンスセンター 大阪けいさつ病院、独立行政法人 労働者健康安全機構 関西ろうさい病院、地方独立行政法人大阪府立病院機構 大阪急性期・総合医療センター、独立行政法人 地域医療機能推進機構 大阪病院、独立行政法人 国立病院機構 大阪医療センター、地方独立行政法人 りんくう総合医療センター、八尾市立病院、医療法人渡辺医学会 桜橋渡辺未来医療病院


Other administrative information

Date of disclosure of the study information

2026 Year 05 Month 25 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

2025 Year 08 Month 19 Day

Date of IRB

2025 Year 09 Month 01 Day

Anticipated trial start date

2026 Year 05 Month 22 Day

Last follow-up date

2031 Year 03 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Arrhythmia recurrence after catheter ablation will be assessed as the primary endpoint.


Management information

Registered date

2026 Year 05 Month 22 Day

Last modified on

2026 Year 05 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000068703