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RecruitingNCT04183660

A Post Market Surveillance Study of the Hemovent Extracorporeal Cardiopulmonary Support System:The MOBYBOX Trial

A Post Market Surveillance Study of the Hemovent Extracorporeal Cardiopulmonary Support System for Cardiac and Respiratory Support: The MOBYBOX Trial

Status
Recruiting
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Hemovent GmbH · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate prospectively the safety and performance of the MOBYBOX System in the veno-arterial configuration in patients with cardiorespiratory failure or in the veno-venous configuration in patients with severe respiratory failure.

Conditions

Interventions

TypeNameDescription
DEVICEMOBYBOX Systemextracorporeal cardiopulmonary support

Timeline

Start date
2024-04-30
Primary completion
2026-04-01
Completion
2026-12-01
First posted
2019-12-03
Last updated
2025-05-31

Locations

4 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT04183660. Inclusion in this directory is not an endorsement.

A Post Market Surveillance Study of the Hemovent Extracorporeal Cardiopulmonary Support System:The MOBYBOX Trial (NCT04183660) · Clinical Trials Directory