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
| Type | Name | Description |
|---|---|---|
| OTHER | Invasive ventilation | Invasive 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.