Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation

PHASE3TerminatedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

June 30, 2005

Primary Completion Date

December 31, 2006

Study Completion Date

December 31, 2006

Conditions
Atrial Fibrillation
Interventions
DEVICE

Flex 4 and Generator

Trial Locations (21)

10021

Lenox Hill Hospital, New York

14642

Univesity of Rochester Medical, Rochester

22908

University of VIrginia Health System, Charlottesville

30309

Piedmont Hospital, Atlanta

37232

Vanderbilt University Medical Center, Nashville

46202

Methodist Hospital, Indianapolis

46237

St. Francis Hospital and Health Center, Indianapolis

48910

Alegent Health, Omaha

53210

Wisconsin Heart Hospital, Milwaukee

54401

Wausau Heart and Lung Surgeons, Wausau

75230

Cardiopulmonary Research Science and Technology Institute, Dallas

75246

Baylor University, Dallas

76104

Plaza Medical Center, Fort Worth

90027

Kaiser Permanente Los Angeles Medical Center, Los Angeles

90806

Long Beach Memorial Medical Center, Long Beach

92037

Scripps Memorial/ Kaiser Permanente, La Jolla

95819

Mercy General Hospital, Sacramento

97225

Providence St. Vincent Medical Center, Portland

98111

Virginia Masonic Clinic, Seattle

07102

St. Michael's Medical Center, Newark

07450

Valley Hospital, Ridgewood

Sponsors
All Listed Sponsors
lead

Boston Scientific Corporation

INDUSTRY