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Clinical Trial Details — Status: Approved for marketing

Administrative data

NCT number NCT00733447
Other study ID # RA-142
Secondary ID P030011
Status Approved for marketing
Phase N/A
First received August 11, 2008
Last updated July 28, 2015
Start date March 2010
Est. completion date May 2014

Study information

Verified date July 2015
Source SynCardia Systems. Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationUnited States: Institutional Review Board
Study type Expanded Access

Clinical Trial Summary

The purposes of this study are to confirm that the Freedom Driver System is a suitable pneumatic driver for clinically stable TAH-t subjects, and that patients and lay caregivers can be trained to manage the Freedom Driver System safely outside the hospital.


Recruitment information / eligibility

Status Approved for marketing
Enrollment 0
Est. completion date May 2014
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who are implanted with the TAH-t and are clinically stable.

Exclusion Criteria:

- Patients who are implanted with the TAH-t and are not clinically stable.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Device:
CardioWest temporary Total Artificial Heart (TAH-t) System
The SynCardia CardioWest temporary Total Artificial Heart (TAH-t) System is a pulsatile biventricular device that replaces a patient's native ventricles and valves, and pumps blood to both pulmonary and systemic circulation. The system consists of the implantable CardioWest TAH-t and an external pneumatic driver connected by drivelines.

Locations

Country Name City State
United States Hospital of the University of Pennsylvania Philadelphia Pennsylvania
United States Mayo Clinic Hospital Phoenix Arizona
United States Virginia Commonwealth University Medical Center Richmond Virginia

Sponsors (1)

Lead Sponsor Collaborator
SynCardia Systems. Inc.

Country where clinical trial is conducted

United States, 

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06174103 - BiVACOR® Total Artificial Heart Early Feasibility Study N/A
Recruiting NCT03659851 - Levosimendan In Patients Undergoing LVAD Implantation
Completed NCT00614510 - SynCardia CardioWest TAH-t Postmarket Surveillance Study N/A