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COMPLETED Phase 4

A Comparison of Antiarrhythmic Drug Therapy and Radio Frequency Catheter Ablation in Patients With Paroxysmal Atrial Fibrillation

NCT00540787 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare radiofrequency catheter ablation and antiarrhythmic drug treatment for the maintenance of sinus rhythm in paroxysmal atrial fibrillation patients.

Interventions

  • DEVICE Radiofrequency ablation, antiarrhythmic drugs
  • DRUG Amiodarone, flecainide, propafenone, quinidine, dofetilide, sotalol, cibenzoline, beta blocking and calcium channel blocking agents and antiarrhythmic drugs
  • DEVICE ThermoCool Radiofrequency Catheter

Study Locations (6)

Other

  • Hopital Lariboisiere — Paris
  • Hopital Cantonal de Geneve — Geneva

Alabama

  • University of Alabama, Birmingham — Birmingham

Massachusetts

  • Massachusetts General Hospital — Boston

Ohio

  • Mid-Ohio Cardiology — Columbus

Paris

  • Hôpital Haut Lèvêque — Pessac

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 2003-08-01
Est. Completion 2006-06-01
Phase Phase 4

Sponsor

Biosense Webster

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00540787

The ClinicalTrials.gov registry entry for NCT00540787 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 112 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Biosense Webster, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Paroxysmal Atrial Fibrillation appearing as the primary indexed condition, and to 3 interventions — of which Radiofrequency ablation, antiarrhythmic drugs is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00540787 reports 6 study locations spanning 5 distinct geographic areas — top geographies include Other, Alabama, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00540787 about?

NCT00540787 is a clinical study titled "A Comparison of Antiarrhythmic Drug Therapy and Radio Frequency Catheter Ablation in Patients With Paroxysmal Atrial Fibrillation". The purpose of this study is to compare radiofrequency catheter ablation and antiarrhythmic drug treatment for the maintenance of sinus rhythm in paroxysmal atrial fibrillation patients.

What is the current status of trial NCT00540787?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 112 participants. The study started on 2003-08-01. Estimated completion is 2006-06-01.

What conditions does trial NCT00540787 study?

This clinical trial studies the following conditions: Paroxysmal Atrial Fibrillation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00540787?

The interventions under investigation include: Radiofrequency ablation, antiarrhythmic drugs (DEVICE), Amiodarone, flecainide, propafenone, quinidine, dofetilide, sotalol, cibenzoline, beta blocking and calcium channel blocking agents and antiarrhythmic drugs (DRUG), ThermoCool Radiofrequency Catheter (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00540787?

This trial is sponsored by Biosense Webster, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00540787 being conducted?

This trial has 6 study locations across Alabama, Massachusetts, Ohio, Paris. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial