Personalized Mechanical Ventilation Guided by UltraSound in Patients With Acute Respiratory Distress Syndrome

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Rationale Acute respiratory distress syndrome (ARDS) is a frequent cause of hypoxemic respiratory failure with a mortality rate of approximately 30%. The identification of ARDS phenotypes, based on focal or non-focal lung morphology, can be helpful to better target mechanical ventilation strategies of individual patients. Lung ultrasound (LUS) is a non-invasive tool that can accurately distinguish 'focal' from 'non-focal' lung morphology. The investigators hypothesize that LUS-guided personalized mechanical ventilation in ARDS patients will lead to a reduction in 90-day mortality compared to conventional mechanical ventilation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Admitted to a participating ICU,

• invasively ventilated and

• fulfil the Berlin criteria for moderate or severe ARDS.

Locations
Other Locations
Belgium
Chu-Brugmann
RECRUITING
Brussels
Denmark
Bispebjerg Hospital
RECRUITING
Copenhagen
Nordsjaellands Hospital
RECRUITING
Hillerød
Greece
Evaggelismos Hospital
RECRUITING
Athens
Ireland
Galway University Hospitals
RECRUITING
Galway
Italy
Ospedale Generale Regionale F. Miulli
RECRUITING
Acquaviva Delle Fonti
Azienda Ospedaliero Universitaria Consorziale Policlinico di Bari
RECRUITING
Bari
Netherlands
Amsterdam UMC, location AMC
RECRUITING
Amsterdam
Amsterdam UMC, location VUmc
RECRUITING
Amsterdam
Poland
Centralny Szpital Kliniczny MSWiA
RECRUITING
Warsaw
Contact Information
Primary
Jante S Sinnige, M.D.
j.s.sinnige@amsterdamumc.nl
+31637405311
Backup
Marry R Smit, Dr.
m.r.smit@amsterdamumc.nl
+3120 5666339
Time Frame
Start Date: 2022-08-09
Estimated Completion Date: 2027-11-01
Participants
Target number of participants: 538
Treatments
Experimental: Personalized ventilation
If a patient is assigned to the intervention group, ventilator settings will be adjusted based on the lung morphology (focal or non focal) results of the lung ultrasound.
Active_comparator: Standard care
Patients assigned to the control group will be ventilated according to the current standard of care.
Sponsors
Leads: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

This content was sourced from clinicaltrials.gov