Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05719259

Perpetual Observational Study - Ventilator Associated Pneumonia

POS-VAP: Perpetual Observational Study - Ventilator Associated Pneumonia

Status
Recruiting
Phase
Study type
Observational
Enrollment
20,000 (estimated)
Sponsor
European Clinical Research Alliance for Infectious Diseases (ECRAID) · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Ventilator-Associated Pneumonia (VAP) is a bacterial respiratory infection that patients in the Intensive Care Unit (ICU) often get when they cannot breathe for themselves and require mechanical ventilation. It is linked to higher chances of death, a longer stay in the hospital, higher costs, and the use of more antibiotics. Options to help prevent or treat this disease are in development and will require evaluation in future clinical trials. The goal of POS-VAP is to build and continuously train a network of ICUs to be prepared for doing these trials, to facilitate their execution.

Detailed description

Ventilator associated pneumonia (VAP) is one of the most frequent healthcare associated infections in the Intensive Care Unit (ICU) and a significant burden among ICU patients under invasive mechanical ventilation (IMV). Several preventive and therapeutic treatment options are being developed in the field of VAP that will require evaluation in future randomized controlled trials (RCTs). RCTs are the gold standard for evaluating medical interventions but are difficult to perform in a population at risk of, or with, VAP. These trials are challenging since it is difficult to recruit a large enough volume of high-quality centers to achieve the required number of recruited patients, especially if the focus is on specific patient groups (e.g., VAP due to a specific pathogen), for which site selection can be even more challenging and time consuming. There is a need for a well-organized and well-trained international network of ICUs focusing on VAP research that enables efficient execution of RCTs on diagnostic, preventive and curative interventions in this population. Through a Perpetual Observational Study (POS) we can provide quick access to a network of sites that fulfill pre-specified criteria. Additionally, the structured network of POS sites within ECRAID will maintain continuous activity to carry out observational studies in this specific field, implementing informed consent (where required), increasing quality and efficiency, and facilitating contracting.

Conditions

Timeline

Start date
2022-08-03
Primary completion
2025-12-01
Completion
2026-03-01
First posted
2023-02-08
Last updated
2024-04-15

Locations

35 sites across 13 countries: Albania, Belgium, Croatia, Czechia, France, Germany, Greece, Italy, Netherlands, Romania, Serbia, Spain, United Kingdom

Source: ClinicalTrials.gov record NCT05719259. Inclusion in this directory is not an endorsement.