A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+
NCT: NCT07326215 · RECRUITING
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.