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Clinical Trial Summary

Hong Kong and Taiwan HM3 PMS is a prospective, single arm, post market surveillance is designed to evaluate clinical and functional outcomes with the HM3 LVAS as a treatment for advanced heart failure. The PMS will enroll approximately 30 patients, that meet the HM3 commercially approved labelling indications, from approximately 4 sites in Hong Kong and Taiwan. PMS participants will be followed until the 24 months follow-up visit or until they experience an outcome, whichever comes first.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04703855
Study type Interventional
Source Abbott Medical Devices
Contact
Status Terminated
Phase N/A
Start date July 14, 2021
Completion date June 30, 2022

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