Critical Care Medicine

3

Review clinical trials related to Critical Care Medicine. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

UP STUDY - Decipher Persistent Critical Illness Through in Deep Clinical Phenotyping.

Persistent Critical Illness (PCI) is a condition that affects some patients who remain in the Intensive Care Unit (ICU) for a long time, usually more than 10-14 days. It is estimated to occur in 5-20% of critically ill patients. A recent Portuguese study found that more than 14% of ICU patients stayed longer than 14 days. PCI is often associated with ongoing need for life support, such as mechanical ventilation or medications to maintain blood pressure. However, patients may also experience severe muscle weakness, repeated infections, or other complications, which makes this group very diverse. One of the main risk factors for prolonged ICU stay is sepsis, a severe infection that affects the whole body. Other factors-such as prior health conditions, use of corticosteroids, sedation practices, early versus late mobilization, fluid and antibiotic management, and delirium treatment-may also influence the development and course of PCI. This study aims to identify different clinical patterns ("clusters") among critically ill patients who remain in the ICU for more than 10 days. Patients will be followed until hospital discharge, and up to one year if data are available. Understanding these different patterns will help develop more personalized and effective care strategies for each patient profile. The study is a multicenter retrospective cohort including adult patients (≥18 years) admitted to participating ICUs for more than 5 days between 2021 and 2023. Data collected will include demographic, clinical, and laboratory information, details of organ support (such as mechanical ventilation or vasopressors), medications, nutrition, and rehabilitation practices. Statistical and machine learning methods will be used to identify groups of patients with similar clinical trajectories and to assess how these groups are related to outcomes such as survival, recovery of organ function, or long-term disability. Expected results are the identification of distinct clinical clusters of PCI that combine clinical and laboratory data, and the development of tailored management strategies to improve recovery and outcomes for patients with PCI.

Participants needed: 7,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Lisbon Academic Medical Center - Centro Académico de Medicina de LisboaUpdated: Apr 13, 2026Locations: 7
Eligibility criteria

Adult patients aged 18 years or older; [+1]

Patients with an ICU stay < 5 days; [+2]

Status: Recruiting

Pediatric Intensive Care Transport Registry

The aim is to establish a nationwide registry for pediatric intensive care transports in Germany. The project aims to describe and analyse the need for, and current practice of, specialised transports. These data could then be used for future demand planning.

Participants needed: 1,000
Trial details
Age: 27-17Biological sex: AllType: ObservationalSponsor: Philipps University MarburgUpdated: Jul 20, 2025Locations: 2Duration: 1 Day
Eligibility criteria

Critically ill children aged at least 27 days and a corrected gestational age of... [+5]

Status: Not yet recruiting

Evaluating the Clinical Effectiveness of "Endotracheal Tube Position Anomaly Alerting System"

The goal of this clinical trial is to determine whether the Endotracheal Tube Position Anomaly Alerting System (ETPAAS) effectively reduces the duration of endotracheal tube malposition in patients admitted to the intensive care unit (ICU). Additionally, the study will assess the clinical impact, usability, and user satisfaction of ETPAAS. The main questions it aims to answer are: * Does ETPAAS reduce the duration of endotracheal tube malposition? * What are healthcare workers' perspectives on the usability and satisfaction of ETPAAS? Participants will receive standard care, with or without ETPAAS, in the intensive care unit. Researchers will evaluate the duration of endotracheal tube malposition. Healthcare workers will complete a questionnaire assessing the usability and satisfaction of ETPAAS.

Participants needed: 200
Trial details
Biological sex: AllType: InterventionalSponsor: Kaohsiung Medical University Chung-Ho Memorial HospitalUpdated: Mar 4, 2025Locations: 1
Eligibility criteria

Patients admitted to the intensive care unit [+1]

Patients disagree to participate in the study