Novel ECCO2R Device for Hypercapnic Respiratory Failure

Status Recruiting

Clinical Trial Summary

The objective of this study is to assess the efficacy and safety of this new Prismalung+ membrane in its intended clinical setting by demonstrating a reduction in ventilatory parameters and pulmonary energy load or the successful maintenance of spontaneous breathing, respectively, the absence of the need to initiate vv-ECMO therapy, and initial survival.

Clinical Trial Description

Our hypotheses are that decarboxylation therapy by means of the novel Prismalung+ membrane in patients with hypercapnic respiratory failure (I) allows the reduction of tidal volume, peak airway pressure, dP and pulmonary energy load (as measured by AUC over 72 hours) as compared to baseline in mechanically ventilated patients OR is associated with successful continuation of spontaneous breathing despite respiratory exhaustion (no decision to intubate), and that these patients (II) warrant no decision to initiate vv-ECMO therapy and (III) do not experience early mortality. The primary Objectives of the study are to test our hypotheses I to III by applying the novel Prismalung+ ECCO2R device in mechanically ventilated patients and spontaneously breathing patients experiencing hypercapnic respiratory failure in a multi-central prospective trial in three experienced intensive care units in Switzerland. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05316532
Study type	Observational
Source	University of Zurich
Contact	Stefanie Keiser, Dr. Sc. nat.
Phone	+41797956912
Email	stefanie.keiser@usz.ch
Status	Recruiting
Phase
Start date	June 5, 2023
Completion date	December 31, 2025

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