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COMPLETED NA

Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures

NCT02274857 · View on ClinicalTrials.gov ↗

Study Summary

The study is a prospective, multicenter, randomized study to assess the safety and effectiveness of FIRM procedures followed by conventional ablation including PVI versus a standard PVI procedure for the treatment of persistent atrial fibrillation (AF).

Interventions

  • PROCEDURE Standard PVI Ablation
  • PROCEDURE FIRM-Guided Procedure and PVI

Study Locations (18)

Other

  • Unfallkrankenhaus Berlin — Berlin
  • Klinikum Coburg GmbH — Coburg
  • Zentrum für klinische Prüfungen in der Facharztzentrum Dresden-Neustadt GbR — Dresden
  • Städtisches Klinikum Karlsruhe gGmbH — Karlsruhe
  • Leipzig Heart Institute GmbH — Leipzig
  • Kardiologische Gemeinschaftspraxis am Park Sanssouci — Potsdam
  • Erasmus Medical Center — Rotterdam

Indiana

  • Indiana University - Krannert Institute of Cardiology — Indianapolis
  • St. Vincent Hospital — Indianapolis

Arizona

  • Arizona Heart Rhythm Center — Phoenix

California

  • Hoag Memorial Hospital Presbyterian — Newport Beach

Illinois

  • Loyola University Medical Center — Maywood

Maryland

  • The Johns Hopkins Hospital — Baltimore

New Jersey

  • Hackensack UMC — Hackensack

New York

  • Weill Medical College at Cornell University — New York

Trial Details

FieldValue
Enrollment Target 350 participants
Start Date 2014-10
Est. Completion 2018-11-10
Phase NA

Sponsor

Abbott Medical Devices

155 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02274857

The ClinicalTrials.gov registry entry for NCT02274857 describes a study currently listed as completed. It is categorized as NA, 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 350 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 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 Persistent Atrial Fibrillation appearing as the primary indexed condition, and to 2 interventions — of which Standard PVI Ablation 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: NCT02274857 reports 18 study locations spanning 11 distinct geographic areas — top geographies include Other, Indiana, Arizona. 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 NCT02274857 about?

NCT02274857 is a clinical study titled "Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures". The study is a prospective, multicenter, randomized study to assess the safety and effectiveness of FIRM procedures followed by conventional ablation including PVI versus a standard PVI procedure for the treatment of persistent atrial fibrillation (AF).

What is the current status of trial NCT02274857?

This trial is currently completed. It is a NA study. The enrollment target is 350 participants. The study started on 2014-10. Estimated completion is 2018-11-10.

What conditions does trial NCT02274857 study?

This clinical trial studies the following conditions: Persistent 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 NCT02274857?

The interventions under investigation include: Standard PVI Ablation (PROCEDURE), FIRM-Guided Procedure and PVI (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02274857?

This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02274857 being conducted?

This trial has 18 study locations across Arizona, California, Illinois, Indiana, Maryland. 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