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Critically Ill clinical trials

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NCT ID: NCT05467332 Not yet recruiting - Clinical trials for Acute Respiratory Failure

Tracheal Positive Pressure During High Flow Nasal Oxygen Administration in Critically Ill Patients: a Physiologic Study.

HPEEP
Start date: April 2023
Phase:
Study type: Observational

High flow nasal cannula administration in critically ill patients is frequently used to improve acute respiratory failure or to prevent respiratory failure after extubation. It acts generating a mild positive pressure in the airways and by reducing respiratory effort of patients. However to the best of our knowledge, no study to date has directly measured the amount of positive pressure generated in the trachea of patients. The primary aim, therefore, of this study measures this positive pressure after extubation in critically ill patients.

NCT ID: NCT05112406 Not yet recruiting - Sepsis Clinical Trials

Early Diagnostic Biomarkers of Sepsis

Start date: December 2021
Phase:
Study type: Observational

A Comparison between CRP, ferritin, and serum zinc as early diagnostic biomarkers of sepsis in critically ill patients

NCT ID: NCT04502511 Not yet recruiting - Critically Ill Clinical Trials

Heterogeneity of Critical Illness: a Cohort Study

HEALICS
Start date: October 1, 2020
Phase:
Study type: Observational [Patient Registry]

Rationale: There is large heterogeneity in disease states of critically ill patients at ICU admittance and there is also large heterogeneity in their disease severity during ICU stay. Still, some patients may show remarkable similarities in disease patterns. There is a lack of understanding of causal mechanisms that lead to divergent outcomes in critically ill patients, and at the same time different diseases may share common underlying, yet unidentified, causal pathways that could explain similarities between different diseases. Objective: To explore the association between patient characteristics and the severity of organ failure in critically ill patients admitted to the ICU Study design: Prospective cohort study Study population: Adult critically ill patients in the ICU Intervention (if applicable): not applicable Main study parameters/endpoints: Maximum severity of organ failure observed during ICU stay measured by the maximum SOFA score and quality of life at one year follow-up

NCT ID: NCT03596853 Not yet recruiting - Critically Ill Clinical Trials

Progressive Mobilization With Dose Control and Training Load in in Critically Ill Patients

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

Immobilization and bed rest of patients in intensive care units (ICU) increases their risk for muscle dysfunction and prolonged mechanical ventilation, leading to physical deconditioning and loss of functionality. Active mobilization is a therapeutic strategy that typically involves exercises in which the patient uses his or her own strength and muscular control, is a feasible, safe, and low-cost intervention to improve muscle dysfunction and disability in patients at the ICU. Despite scientific advances, the current description and prescriptions of exercises at the ICU remain incomplete with respect to the control and the description of the variables of training load (volume and intensity), programming, and progression.

NCT ID: NCT03438201 Not yet recruiting - Cancer Clinical Trials

Protein Intake Associated With Physical Activity Related to Specific Outcomes

STRENGTH
Start date: April 4, 2018
Phase: N/A
Study type: Interventional

This is a Randomized Controlled Trial . The purpose of this study is to assess the hypothesis that whether a high protein diet combined with a physical activity protocol in surgical cancer patients admitted to the ICU in the post operative period is associated with better physical function at the hospital discharge as well as a better quality of life.

NCT ID: NCT03019900 Not yet recruiting - Anemia Clinical Trials

Survey of Blood Transfusion Practices in Critically Ill Patients at High Altitude

Start date: February 2017
Phase: N/A
Study type: Observational

The purpose of this study is to describe current practice on red blood cell transfusion in critically ill patients of intensive care units located in high altitude areas

NCT ID: NCT01482988 Not yet recruiting - Critically Ill Clinical Trials

Role of Polymorphisms in the Dectin-1 Gene in Determining the Risk of Candida Colonization and Infection in Critically Ill Patients

Dectin-1
Start date: December 2011
Phase: N/A
Study type: Observational

The principal aim of this study is to establish if a polymorphism in a gene important for innate immunity to fungi represents a significant risk factor for the development of Candida colonisation and subsequent invasive candidosis in critically ill patients. Incorporation of a screening programme onto a risk-based algorithm for critical care patients would allow more effective targeting of molecular diagnostic tests, anti-fungal prophylaxis and targeted treatment. Sequential critical care patients will be screened for gene polymorphisms and undergo regular screening for Candida colonization.

NCT ID: NCT00916591 Not yet recruiting - Critically Ill Clinical Trials

Prokinetic Drugs and Enteral Nutrition

prokinetics
Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to compare the effect of two drugs that can help in the prevention of regurgitation during the administration of enteral nutrition and define which one is the most effective.

NCT ID: NCT00894309 Not yet recruiting - Critically Ill Clinical Trials

Validation of the Fluid Responsiveness Index in Critically Ill Patients

FRI
Start date: May 2009
Phase: N/A
Study type: Observational

Fluid therapy is an important part of the management of patients with hemodynamic instability in the intensive care unit. By increasing cardiac preload, it aims at elevating cardiac output (CO) and thus restoring hemodynamic conditions in patients who are preload responsive. By contrast, volume administration can be deleterious in terms of pulmonary edema formation or other manifestations or fluid overload, especially in patients who are not preload responsive. Functional dynamic parameters that use heart-lung interactions, such as pulse pressure variation (PPV) and stroke volume variation (SVV) are considered accurate predictors of preload responsiveness in patients receiving fully controlled mechanical ventilation. However, in cases of spontaneous breathing activity where heart-lung interaction indices fail to predict fluid responsiveness, one needs parameters able to reliably predict the hemodynamic response of fluid administration. A new index that could indicate fluid responsiveness, so-called the fluid responsiveness index (FRI), has been elaborated. The advantage is that it could be used in patients who are not in control mechanical ventilation as well as in patients who are fully adapted to mechanical ventilation. The FRI is based upon the analysis of continuous arterial and continuous central venous pressure. The FRI is determined by the relation of cardiac and respiratory activity; both are evaluated by means of power spectrum analysis of the pressures recorded. The aim of this study is to test the value of the FRI to predict the hemodynamic response to fluid infusion in patients with hemodynamic instability not receiving fully controlled mechanical ventilation.