Atrial Fibrillation Ablation Device Comparison Study

PHASE4WithdrawnINTERVENTIONAL
0
Timeline

Start Date

April 30, 2007

Primary Completion Date

November 20, 2008

Study Completion Date

May 31, 2009

Conditions
Atrial Fibrillation
Interventions
DEVICE

Dry bipolar radiofrequency (RF) clamp

Specified device used for ablation during standard surgical procedure

DEVICE

Unipolar microwave antenna

Specified device used for ablation during standard surgical procedure

DEVICE

Unipolar cryothermic probe

Specified device used for ablation during standard surgical procedure

DEVICE

Irrigated unipolar RF antenna

Specified device used for ablation during standard surgical procedure

DEVICE

Irrigated bipolar RF clamp

Specified device used for ablation during standard surgical procedure

DEVICE

Hi-intensity focused ultrasound wand

Specified device used for ablation during standard surgical procedure

Trial Locations (1)

11219

Maimonides Medical Center, Brooklyn

Sponsors
All Listed Sponsors
lead

Maimonides Medical Center

OTHER

NCT00466973 - Atrial Fibrillation Ablation Device Comparison Study | Biotech Hunter | Biotech Hunter