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Trial · NCT04942834

Using Cryoballoon Ablation as Initial Treatment for Persistent Atrial Fibrillation

NCT04942834, Not applicable, Completed, Ruijin Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Using Cryoballoon Ablation as Initial Treatment for Persistent Atrial Fibrillation. Trials, record NCT04942834. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04942834

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Using Cryoballoon Ablation as Initial Treatment for Persistent Atrial Fibrillation
NCT number
NCT04942834
Status
Completed
Phases
Not applicable
Enrollment
320 participants, actual
Lead sponsor
Ruijin Hospital
Conditions
Atrial Fibrillation, Persistent, Arrhythmias, Cardiac
Interventions
Antiarrhythmic drug including Propafenone, Sotalol, Dronedarone and Amiodarone, cryoballoon ablation
First posted
2021-06-29
Last updated
2026-08-18

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTreatment success at 12 monthsRandomization to 12 months
Treatment success at 12 months after antiarrhythmic drug (AAD) initiation or ablation utilizing cryoballoon catheter measured by freedom from AF recurrence following a 3-month period after the index ablation or AAD initiation(Dynamic ECG requires a minimum of 30 seconds, while a 12-lead ECG requires at least 10 seconds.).
SecondaryQuality of life changes at 12 months measured by AFEQTone yearThe improvement in quality of life between baseline and 12 months after the index ablation procedure or AAD measured by AF Quality of Life Survey (AFEQT)
SecondaryQuality of life changes at 12 months measured by SF-12one yearThe improvement in quality of life between baseline and 12 months after the index ablation procedure or AAD measured by 12-Item Short Form Survey (SF-12)
SecondaryArrhythmia recurrence during blanking period3 monthsatrial tachycardia recurrence rate during the blanking period
Secondarytime to first time cardiovascular hospitalization (month)one yeartime to first time cardiovascular hospitalization after treatment (month)
SecondaryRate of serious procedure-related and serious cryoablation system-related reported adverse eventsone yearRate of serious procedure-related and serious cryoablation system-related reported adverse events through 12 months after the index ablation procedure

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
42677894DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04942834

GET https://conductscience.org/api/trials/v1/NCT04942834/registered