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nContactSurgical Numeris-AF Tethered Coagulation System for Treatment of Persistent & LSP AF

NCT00950092 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2014-04-03

No results posted yet for this study

Summary

This is a multi center, non-randomized, prospective, open label, clinical trial evaluating the safety and efficacy of the nContact Surgical Numeris-AF Tethered Coagulation System when used to treat patients with persistent and longstanding persistent AF during concomitant cardiac surgery.

Conditions

Interventions

DEVICE

Numeris-AF Tethered Coagulation System with VisiTrax

Surgical radiofrequency (RF) epicardial ablation using the nContact Numeris-AF Tethered Coagulation System

Sponsors & Collaborators

  • nContact Surgical Inc.

    lead INDUSTRY

Principal Investigators

  • Edward Garrett, M.D. · Baptist Memorial Hospital - Memphis

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2013-06-30
Completion
2013-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00950092 on ClinicalTrials.gov