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Clinical Trial

A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+

NCT: NCT07326215 · RECRUITING

NCT IDNCT07326215
StatusRECRUITING
Start Date2025-12-11
Completion2027-02-28
SponsorVantive Health LLC (INDUSTRY)
First posted
Last updated

Brief Summary

PrismaLung+ is a sterile, single-use medical device aimed at performing partial removal of carbon dioxide (CO2) from the patient's venous blood via diffusion through a membrane. The goal of this prospective, open label, randomized controlled study is to evaluate the efficacy and safety of PrismaLung+ on extracorporeal carbon dioxide removal (ECCO2R) in critically ill patients under invasive mechanical ventilation (IMV). Patients will be randomized to receive either IMV combined with ECCO2R (using PrismaLung+) in the study group or IMV alone in the control group, at a ratio of 2:1.

Frequently Asked Questions

What is A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+?

A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+ is a clinical trial registered under NCT07326215. Current status: RECRUITING.

What is the status of NCT07326215?

The current status of NCT07326215 (A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+) is: RECRUITING.

When did A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+ start?

A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+ started on 2025-12-11.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.