TactiCath Post Market Approval Study | Clinical Research Studies Listing

Recruiting

18 years - 100 years

All

Phase 4

35 participants needed

1 Location

Brief description of study

The purpose of the research study is to obtain additional information safety and effectiveness of an FDA approved catheter when used to treat patients with Paroxysmal atrial fibrillation.

Detailed description of study

The purpose of the study is to provide data and safety for the Food and Drug administration (FDA). The study is designed for patients with paroxysmal atrial fibrillation. Participants will only be enrolled if at the time of consent present with paroxysmal atrial fibrillation and meet criteria for an ablation procedure. The study is seeking participants willing to be followed for a period of 5 years

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Atrial Fibrillation
Age: 18 years - 100 years
Gender: All

Updated on 19 Feb 2024. Study ID: 821652

Find a site

Your Information has been sent successfully.

Message sent successfully.

We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.

If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.

Send a message

Enter your contact details to connect with study team

View email

Phone

View phone

First name*

Last name*

Email*

Phone number*

Preferred way of contact

Race

Ethnicity

Are you Healthy Volunteer

Other language

By sending a message, I agree that my data will be sent to a representative for the selected site and processed in accordance with this website's Privacy Policy (see link in footer).

Message For Non Enrolling By Invitation Trial

Select a study center that’s convenient for you, and get in touch with the study team.