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Terminated Phase 3 Interventional

Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation

ClinicalTrials.gov ID: NCT00111488

Public ClinicalTrials.gov record NCT00111488. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 1:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Study of Surgical Ablation With Microwave Energy for the Treatment of Atrial Fibrillation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the Randomized Study of Surgical Ablation with Microwave Energy for the Treatment of Atrial Fibrillation (RESOLVE-AF) trial is to determine the safety and effectiveness of the Guidant FLEX® Microwave Surgical Ablation System in the treatment of permanent atrial fibrillation (AF).

Study identification

NCT ID
NCT00111488
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boston Scientific Corporation
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2005 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Jan 6, 2016

2005 – 2006

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Scripps Memorial/ Kaiser Permanente La Jolla California 92037 —
Long Beach Memorial Medical Center Long Beach California 90806 —
Kaiser Permanente Los Angeles Medical Center Los Angeles California 90027 —
Mercy General Hospital Sacramento California 95819 —
Piedmont Hospital Atlanta Georgia 30309 —
Methodist Hospital Indianapolis Indiana 46202 —
St. Francis Hospital and Health Center Indianapolis Indiana 46237 —
Alegent Health Omaha Nebraska 48910 —
St. Michael's Medical Center Newark New Jersey 07102 —
Valley Hospital Ridgewood New Jersey 07450 —
Lenox Hill Hospital New York New York 10021 —
Univesity of Rochester Medical Rochester New York 14642 —
Providence St. Vincent Medical Center Portland Oregon 97225 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Cardiopulmonary Research Science and Technology Institute Dallas Texas 75230 —
Baylor University Dallas Texas 75246 —
Plaza Medical Center Fort Worth Texas 76104 —
University of VIrginia Health System Charlottesville Virginia 22908 —
Virginia Masonic Clinic Seattle Washington 98111 —
Wisconsin Heart Hospital Milwaukee Wisconsin 53210 —
Wausau Heart and Lung Surgeons Wausau Wisconsin 54401 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00111488, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 6, 2016 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00111488 live on ClinicalTrials.gov.

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