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NCT06199141: MDR-ECMO

Multi-drug Resistant Gram-negative Bacteria and Veno-venous Extracorporeal Membrane Oxygenation (ECMO)

Completed Last updated 28 February 2024
What this trial tests

trial in Respiratory Distress Syndrome, Adult in 279 participants. Completed in 31 December 2023.

Timeline
1 January 2017
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorUniversity of Padova
StatusCompleted
Study typeOBSERVATIONAL
Enrollment279
Start date1 January 2017
Primary completion31 December 2023
Estimated completion31 December 2023
Sites1 location across Italy

Conditions studied

Sponsor

University of Padova

Who can join

18 and older, any sex, with Respiratory Distress Syndrome, Adult or Multi-antibiotic Resistance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Veno-venous extracorporeal membrane oxygenation (VV-ECMO) is a life-support technique used in patients with most severe acute respiratory distress syndrome (ARDS). ARDS is a life-threatening form of respiratory failure associated with a mortality rate of approximately 40-45%.Despite several studies confirming a real benefit of the use of ECMO in patients with ARDS who are unresponsive to conventional management, ECMO is still a complex and costly treatment that can be exposed to potential complications, such as nosocomial infections (NI).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Respiratory Distress Syndrome, Adult

Currently open trials in the same condition.

Other University of Padova trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06199141.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing