Erasmus Medical Centre
Rotterdam, South Holland, 3015GD, Netherlands
Location status: Recruiting
NCT Number: NCT06757166
To determine whether early endotracheal intubation compared to late endotracheal intubation affects clinical outcome (duration of invasive mechanical ventilation, mortality).
Interested in participating?
Request Info18 year and older
All sexes
Observational
Rotterdam, South Holland, 3015GD, Netherlands
Location status: Recruiting
Non-invasive respiratory support, especially HFNO is usually well-tolerated, especially in COVID-19 patients and can be applied for a prolonged period of time. However, there is a heated debate whether later/delayed endotracheal intubation (due to HFNO / NIV) increases the risk of lung injury, so-called patient self-inflicted lung-injury (P-SILI). The concept of P-SILI assumes that high forces applied to the lung resulting from strenuous breathing effort generated by the patient exacerbates lung-injury and is associated with adverse clinical outcome. It is therefore important to investigate if a longer period of non-invasive respiratory support before invasive mechanical ventilation is associated with adverse clinical outcome. Thus, it is unknown if delaying invasive ventilation worsens clinical outcome. In this study, the research question is whether early compared to late endotracheal intubation improves clinical outcome (duration of invasive mechanical ventilation, mortality)? The aim is to identify the optimal S/F ratio and respiratory rate thresholds for initiating intubation to either improve survival or reduce the duration of invasive ventilation without compromising survival. This is achieved by comparing 25 dynamic treatment regimes defined by combinations of S/F thresholds (<any, 250, 200, 150, 100) and respiratory rate thresholds (>any, 16, 20, 25, 30). Thresholds indicating less severe illness (e.g., S/F < 250 and RR > 16) are considered 'early intubation,' while thresholds indicating more severe illness (e.g., S/F < 100 and RR > 30) are considered 'late intubation'.
Two sensitivity analyses will be conducted:
Additionally, seven subgroup analyses will be conducted:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
endotracheal intubation for invasive mechanical ventilation
Time frame: 28 days
Mortality restricted mean time lost (RMTL) over the 28-day period (area under the cumulative incidence function curve)
Time frame: 28 days
Mortality risk at day 28
Contact information is provided by the study sponsor or research team.
Carmen A.T. Reep, MSc
CONTACT
Evert-Jan Wils, PhD, MD
CONTACT
Erasmus Medical Center
Other
Effects of Early vs. Delayed Invasive Mechanical Ventilation: A Target Trial Emulation
Acronym: NORMO2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.