Safety and Efficacy of Induced Pluripotent Stem Cell-derived Engineered Human Myocardium as Biological Ventricular Assist Tissue in Terminal Heart Failure (BioVAT-DZHK20)

The BioVAT-HF-DZHK20 trial is investigating under which conditions engineered human myocardium is safe to use in the treatment of patients with end-stage heart failure, a condition known as terminal heart failure (NYHA III or IV). To do so, engineered human myocardium will be implanted onto the heart muscle by means of a minimally invasive thoracotomy, a surgical opening of the thorax through an incision between two ribs, or open-heart surgery. With this study, the scientists hope to gain new insights into whether this intervention leads to better heart function, what dosage is the correct one and where the implantation of the artificial heart tissue is most effective.

BioVAT-HF-DZHK20 - Safety and Efficacy of Induced Pluripotent Stem Cell-derived Engineered Human Myocardium as Biological Ventricular Assist Tissue in Terminal Heart Failure (BioVAT-DZHK20)

Publications

There are no publications available yet.

Principal Investigators

Principal investigator: Wolfram-Hubertus Zimmermann (Göttingen)

Study recruitment is available in these cities

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Study information
BioVAT-HF-DZHK20

Recruiting status
Recruiting ongoing
Recruitment start
02.2021
Patients
17
53
Clinical Trials Registrierung

NCT04396899

Category
Early clinical study
DZHK Funding
€ 1.185.447
Links
https://biovat.dzhk.de

Operative contact
Main study center
Florian Walker, MD
biovat.info@med.uni-goettingen.de

Studienzentren/Kontakt (PDF)