Clinical trials

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Condition / disease
Location
Status: Recruiting

Ventilatory Parameters in Acute Neurological Injury

The goal of this observational study is to test the association between baseline ventilatory parameters (in particular mechanical power (MP), mechanical power normalized to predicted body weight (MP/PBW) and driving pressure (DP) with the baseline neurological status (assessed through the Glasgow coma score) in adults patients under mechanical ventilation with acute neurological injury secondary to stroke, brain trauma or subarachnoid hemorrhage. The main question\[s\]it aims to answer are: 1. In patients with acute neurological injury under mechanical ventilation, is there a correlation between the acute neurological injury, assessed using the Glasgow scale on admission, and baseline ventilatory parameters? 2. In patients with acute neurological injury under mechanical ventilation, are the baseline ventilatory parameters altered at baseline?

Participants needed: 19
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: Ramos Mejía HospitalUpdated: Mar 30, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Not listed

Status: Not yet recruiting

Components of Mechanical Power on the Functional Lung in ARDS

Mechanical power (MP) is a composite variable that integrates static and dynamic respiratory parameters and has been associated with ventilator-induced lung injury (VILI). MP is predominantly delivered to the reduced functional lung size, commonly referred to as the "baby lung" (BL). Functional lung size, in turn, is closely related to respiratory system compliance (Crs). Previous studies have demonstrated an association between MP normalized to compliance (MP/Crs) and mortality. Moreover, evidence suggests that VILI associated with MP/Crs results primarily from the combined effect of its components rather than from any single component in isolation. The objective of this study is to evaluate both the overall and the relative contribution of each component of mechanical power, normalized to compliance (MP/Crs), to in-hospital mortality in patients with acute respiratory distress syndrome (ARDS).

Participants needed: 184
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ramos Mejía HospitalUpdated: Dec 4, 2025
Eligibility criteria

Patients ≥ 18 years [+2]

Patients spontaneously breathing [+7]