EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study
NCT: NCT05610787 · ENROLLING_BY_INVITATION
Brief Summary
The purpose of this study is to evaluate the device performance and monitor the safety and effectiveness of the Berlin Heart EXCOR Active Driving System while being used with the approved EXCOR Pediatric Ventricular Assist Device. EXCOR Active Driving System is intended for use with the approved EXCOR Pediatric VAD. The EXCOR Pediatric VAD is intended to provide mechanical circulatory support as a bridge to cardiac transplantation for pediatric patients. Pediatric candidates with severe isolated left ventricular or biventricular dysfunction who are candidates for cardiac transplant and require circulatory support may be treated using the EXCOR Pediatric. EXCOR Active is intended for use in a clinical setting. EXCOR Active can be used in any kind of hospital unit (e.g. OR, ICU, intermediate care unit or general care unit). The driving unit may be moved between clinical units using the caddy or baby buggy; however, a patient must always be accompanied by a person trained in the use of the manual pump and emergency procedures during transport in the event of an emergency. The driving unit can be transported during operation.
Frequently Asked Questions
What is EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study?
EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study is a clinical trial registered under NCT05610787. Current status: ENROLLING_BY_INVITATION.
What is the status of NCT05610787?
The current status of NCT05610787 (EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study) is: ENROLLING_BY_INVITATION.
When did EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study start?
EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study started on 2022-11-14.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.