Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Influence of Lung Recruitment Potential on PEEP Titration Strategies in ARDS Patients.

Acute Respiratory Distress Syndrome (ARDS) is characterized by severe hypoxemia and diffuse alveolar collapse, often requiring invasive mechanical ventilation. Non-individualized mechanical ventilation settings can cause ventilator-induced lung injury (VILI). Positive end-expiratory pressure (PEEP) prevents alveolar collapse, but its effect varies among individuals. The recruitment-to-inflation (R/I) ratio evaluates bedside lung recruitment potential. This pilot study aims to compare two individualized PEEP titration strategies-one guided by the best static respiratory compliance and another guided by transpulmonary pressure via an esophageal balloon-and evaluate how baseline lung recruitment potential alters the early physiological responses to these interventions. Both strategies are preceded by an identical, standardized pressure-controlled initial lung recruitment maneuver to establish a baseline recruitment state.

Participants needed: 52
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital Dr. Franco Ravera ZuninoUpdated: May 22, 2026
Eligibility criteria

Diagnosis of moderate or severe Acute Respiratory Distress Syndrome (ARDS) accor... [+2]

Evidence of active pulmonary air leaks (bronchopleural fistula, pneumothorax, pn... [+10]

Status: Recruiting

Assessment of the Effect of an Inspiratory Muscle Training Regimen on Decannulation Time in Tracheostomized Subjects

The objective of this project is to evaluate the effect of applying an individualized inspiratory muscle training regimen, combining strength and endurance exercises over a two-week period, on improving maximum inspiratory pressure, diaphragm thickness fraction, and its impact on successful decannulation time in patients with tracheostomy secondary to prolonged mechanical ventilation at HRLBO. Two groups of adult tracheostomized patients will be assessed: an experimental group, who will follow an individualized inspiratory muscle training regimen for 14 days along with standard physiotherapy, and a control group, who will receive standard physiotherapy and guided weaning through scheduled disconnection windows from mechanical ventilation. Both groups will be compared in terms of decannulation time, ICU length of stay, hospital days, and quality of life survey scores. The results of this study will help optimize the management of tracheostomized patients locally and nationally, reducing economic costs for both the country and the patients, and improving their quality of life, contributing to some health objectives for the 2011-2020 decade.

Participants needed: 56
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital Dr. Franco Ravera ZuninoUpdated: Nov 12, 2024Locations: 1
Eligibility criteria

Critically ill patients aged ≥ 18 years [+4]

Limitation of therapeutic effort (LTE*) [+4]