Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:09 PM
Ignite Modification Date:
2025-12-24 @ 11:09 PM
NCT ID:
NCT05898269
Eligibility Criteria:
Inclusion Criteria:
* adult patient (including patient under protective measures/wardship)
* with ARDS as defined by the Berlin criteria
* in the prone position as per international guidelines
* with a calibrated continuous cardiac output monitoring device
* with a clinical indication for a fluid bolus as prescribed by the clinician in charge, and fulfilling at least 2 clinical criteria: mottles, tachycardia, hypotension, drop in cardiac output, oliguria, high arterial lactate concentration, or any other detailed criterion
* with no respiratory efforts
Exclusion Criteria:
* acute cor pulmonale
* patient treated with veno-venous extra-corporeal membrane oxygenation
* hemorrhagic shock
* Child-Pugh C cirrhosis
* death expected to occur in less than 24h
* decision to withhold or suspend active treatments
* intracranial hypertension
* lower limb amputation
* obstruction of the inferior vena cava
* acute abdominal syndrome
* absence of consent to participate
* pregnancy
* patient previously enrolled in the same study
* lack of affiliation to a social security regimen, as per French legislation
* patient deprived of its liberty
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05898269
Study Brief:
Protocol Section:
NCT05898269