Austin, Texas 78705


Purpose:

The objective of the Registry is to provide post market clinical outcome and potential health economics data and confirm the continued safety of the EpiAccess system.


Study summary:

The Registry will be a prospective non-randomized single-arm trial of up to 150 patients enrolled in up to ten (10) centers in the United States. The overall duration of the registry is estimated to be 18 months per site. For the patients the registry duration will be from the time of procedure until discharge from the hospital, estimated to be approximately four (4) days. Prior to enrollment, patients will be evaluated on the basis of the latest available data to establish eligibility. Eligible patients will be considered enrolled in the registry after written informed consent is obtained. As EpiAccess is only used for the access portion of the procedure, the safety performance and effectiveness endpoints are acute from the time of needle insertion until pericardial sac access is achieved. Follow up clinical examinations will be performed according to institutional standard of care. No special tests are required for this device.


Criteria:

Inclusion Criteria: - Patient is 18 years of age or older - Pericardial access is clinically indicated - Patient is willing and able to provide written informed consent Exclusion Criteria: - Patients who have any condition which contraindicates pericardial access or who have any condition specified in the Contraindications section of the Instructions for Use. This includes: - Previous cardiac surgery or myocardial infarctions resulting in pericardial fibrosis - Congenital absence of a pericardium - Absence of a free epicardial space - Patients with active infection - History of chronic pericarditis - Patient requiring anti-arrhythmic drug therapy for the treatment of ventricular arrhythmia - Patient not in normal sinus rhythm - Presence of thrombus in the left atrium - Coagulopathy - Known allergy to contrast media


NCT ID:

NCT02481102


Primary Contact:

Principal Investigator
Andrea Natale, MD
Texas Cardiac Arrhythmia Research Foundation

Claire Williams
Phone: 978-996-4243
Email: claire@dragonconsultinggroups.com


Backup Contact:

Email: pbunes@epiep.com
Pam Bunes
Phone: 864-423-2526


Location Contact:

Austin, Texas 78705
United States

Andrea Natale, MD
Phone: 512-458-9410
Email: tcarfan@gmail.com

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 23, 2017

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