High Power Short Duration Ablation Compared to Moderate Power Long Duration Ablation for Pulmonary Vein Isolation

NCT ID: NCT05959798

Last Updated: 2023-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

204 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-20

Study Completion Date

2023-07-17

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

High Power Short Duration Ablation Compared to Moderate Power Long Duration Ablation for Pulmonary Vein Isolation: safety and acute procedural outcome

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Paroxysmal Atrial Fibrillation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

High power short duration ablation

High power short duration ablation

Intervention Type PROCEDURE

Pulmonary vein isolation by high power short duration radiofrequency catheter ablation

Moderate power long duration ablation

High power short duration ablation

Intervention Type PROCEDURE

Pulmonary vein isolation by high power short duration radiofrequency catheter ablation

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

High power short duration ablation

Pulmonary vein isolation by high power short duration radiofrequency catheter ablation

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* symptomatic, documented, drug-resistent paroxysmal atrial fibrillation
* effective oral anticoagulation

Exclusion Criteria

* any prior left atrial ablation procedure
* presence of left atrial thrombus
* secondary atrial fibrillation due to electrolyte imbalance or thyroid disease
* any prior oesophageal or gastric surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Deutsches Herzzentrum Muenchen

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Isabel Deisenhofer, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

Deutsches Herzzentrum München, Abt. für Elektrophysiologie

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Deutsches Herzzentrum München

München, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

POWER PULSE

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Re-ablation of Persistent Atrial Fibrillation
NCT06845085 NOT_YET_RECRUITING NA