Viewing Study NCT00332371



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Study NCT ID: NCT00332371
Status: TERMINATED
Last Update Posted: 2012-07-09
First Post: 2006-05-31

Brief Title: COMPACT - COMbining Plasma-filtration and Adsorption Clinical Trial
Sponsor: Gruppo Italiano per la Valutazione degli Interventi in Terapia Intensiva
Organization: Gruppo Italiano per la Valutazione degli Interventi in Terapia Intensiva

Study Overview

Official Title: COMPACT COMbining Plasma-filtration and Adsorption Clinical Trial Efficacy and Safety of CPFA Coupled Plasma Filtration Adsorption for Septic Shock in the ICU
Status: TERMINATED
Status Verified Date: 2012-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: The study was prematurely interrupted for futility
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study objective is to clarify whether the application of CPFA coupled plasma-filtration adsorption in addition to the current clinical practice is able to reduce mortality and prevent organ failures in septic shock patients in intensive care unit ICU
Detailed Description: Septic shock is a life-threatening clinical condition characterized by cardiovascular failure as a consequence of infection Septic shock frequently causes multi-organ failure in the ICU For this reason the extracorporeal therapies for the treatment of renal failure have become widespread in the ICU and at the same time new extracorporeal depurative techniques have been developed for the removal of inflammatory mediators One of these techniques is CPFA coupled plasma-filtration adsorption that uses a sorbent once the separation between plasma and blood has been obtained with a plasma filter The study objective is to clarify whether the application of CPFA in addition to the current clinical practice is able to reduce mortality and prevent organ failures in septic shock patients in intensive care unit

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
ISRCTN24534559 None None None