Clinical Trials Directory

Trials / Completed

CompletedNCT06592937

Harmonized and Pooled Database, Named PRIME.

Potentially Modifiable Ventilation Factors Associated With Outcome in Neurocritical Care vs Non-Neurocritical Care Patients - Rational and Protocol for a Patient-Level Analysis of PRoVENT, PRoVENT-iMiC and ENIO (PRIME)

Status
Completed
Phase
Study type
Observational
Enrollment
3,270 (actual)
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers

Summary

We merged the dataset of three large observational studies of invasive ventilation in critically ill patients.

Detailed description

PRIME contains the individual patient data of 3 large observational studies of ventilation, 'PRactice of VENTilation in critically ill patients without ARDS' (PRoVENT), 'PRactice of VENTilation in critically ill patients in Middle-income Countries' (PRoVENT-iMiC) and 'Extubation strategies and in neuro-intensive care unit patients and associations with outcomes' (ENIO).

Conditions

Interventions

TypeNameDescription
OTHERInvasive ventilationInvasive ventilation and respiratory support

Timeline

Start date
2024-01-01
Primary completion
2024-07-26
Completion
2024-07-26
First posted
2024-09-19
Last updated
2024-09-19

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT06592937. Inclusion in this directory is not an endorsement.