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Completed Phase 4 Interventional Results available

Catheter Evaluation for Endocardial Ablation in Patients With Typical Atrial Flutter

ClinicalTrials.gov ID: NCT00318565

Public ClinicalTrials.gov record NCT00318565. 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 Jul 21, 2026, 6:03 PM EDT

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

Official title

Navistar Thermocool Evaluation of the Catheter With the Stockert 70 Radiofrequency Generator for Endocardial Ablation in Patients With Typical Atrial Flutter

Study identification

NCT ID
NCT00318565
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Biosense Webster, Inc.
Industry
Enrollment
291 participants

Conditions and interventions

Conditions

Interventions

  • RF energy delivery for treatment of Typical Atrial flutter Device

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
Dec 31, 2005
Primary completion
Aug 31, 2007
Completion
Jan 31, 2008
Last update posted
Mar 4, 2012

2006 – 2008

United States locations

U.S. sites
23
U.S. states
19
U.S. cities
23
Facility City State ZIP Site status
University of Alabama, Birmingham Birmingham Alabama 35294
Arizona Arrhythmia Consultants Scottsdale Arizona 85251
Good Samaritan Hospital Los Angeles California 90017
Pacific Heart Institute Santa Monica California 90404
University of Florida Gainsville Florida 32611
Memorial Regional Hospital Hollywood Florida 33031
Florida Hospital Orlando Florida 32803
University of Chicago Chicago Illinois 60637
The Care Group LLC, St. Vincent Hospital and Health Care Center, Inc. Indianapolis Indiana 46060
Central Baptist Hospital Lexington Kentucky 40503
Maine Medical Center Portland Maine 04102
University of Maryland Baltimore Maryland 21201
Massachusetts General Hospital Boston Massachusetts 02114
St. John Hospital and Medical Center Detroit Michigan 48236
Park Nicollet Institute Minneapolis Minnesota 55416
Duke University Medical Center Durham North Carolina 27710
University of Oklahoma, Health Sciences Center Oklahoma City Oklahoma 73104
University of Pennsylvania Philadelphia Pennsylvania 19104
Medical University of South Carolina Charleston South Carolina 29425
Texas Heart Institute Houston Texas 77030
University of Vermont, College of Medicine Burlington Vermont 05401
INOVA Research Center Falls Church Virginia 22042
Virginia Commonwealth University Richmond Virginia 23219

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 NCT00318565, 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 Mar 4, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00318565 live on ClinicalTrials.gov.

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