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Critically Ill Patients clinical trials

View clinical trials related to Critically Ill Patients.

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NCT ID: NCT04962204 Recruiting - Clinical trials for Critically Ill Patients

Virtual Visitation in Intensive Care Unit Study

ISEEU
Start date: July 6, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to identify the efficacy of virtual visitation in Intensive Care Unit on patients and their caregivers during COVID-19 Pandemic.

NCT ID: NCT04924920 Recruiting - Clinical trials for Hemodynamic Instability

Sigh35 and End-expiratory Occlusion Test (EEOT) for Assessing flUid Responsiveness in Critically Ill Patients Undergoing Pressure Support Ventilation

SETUP
Start date: February 1, 2022
Phase: N/A
Study type: Interventional

The application of a brief SIGH of 4 seconds at 35 cmH20 has shown to reliably predict fluid responsiveness in critically ill patients undergoing pressure support ventilation. The end-expiratory occlusion test (EEOT) has been also used in the same type of patients, with the same purpose, but in a limited amount of studies. The aim of this study is to compare the reliability of the the two test in assessing fluid responsiveness.

NCT ID: NCT04793568 Active, not recruiting - Clinical trials for Critically Ill Patients

Human Recombinant Interferon Gamma-1b for the Prevention of Hospital-acquired Pneumonia in Critically Ill Patients: a Double-blind, International, Phase 2, Randomized, Placebo-controlled Trial - the PREV-HAP Study

PREV-HAP
Start date: March 29, 2021
Phase: Phase 2
Study type: Interventional

PREV-HAP study is part of a larger project entitled 'Host-targeted Approaches for the Prevention and the treatment of Hospital-Acquired Pneumonia' (HAP2), funded by the European Union's H2020 research and innovation programme under grant agreement N°847782. HAP2 aims to develop stratified host-directed drugs and biomarkers to enhance the prevention and the treatment of HAP and develop precision medicine in infectious diseases. Its ambition is to revolutionize the management of HAP: capitalising on the novel concept of critical-illness related immunosuppression altering the host-pathogens interactions, the aim is to propose a complete reappraisal of the physiopathology of HAP based on the concept of respiratory dysbiosis. The main hypothesis of the PREV-HAP study is that human recombinant Interferon gamma 1b (rHuIFN-γ, Imukin) treatment can restore immunity in critically ill patients and prevent Hospital-Acquired Pneumonia. The hypothesesis is that the in vivo investigations of the host-pathogens interactions can be used for the stratification of patients into high/low risk and responders/non-responders to host-targeted prevention of hospital-acquired infections. The involvement of a state of critical-illness related immunosuppression in the susceptibility to hospital-acquired pneumonia is widely accepted, and an emerging trend is that the development of drugs for the treatment of this acquired immunosuppression will prevent infection and enhance outcomes of hospitalized patients. It has been demonstrated that the productions of IFN-γ by immune cells are decreased in critically ill patients, and that these defects are associated with the susceptibility to HAP. rHuIFN-γ has neither been tested nor is recommended as adjunctive treatment of patients with HAP. Based on these specific factors identified in the host response, it is proposed in this study to use rHuIFN-γ as novel preventive approach for HAP.

NCT ID: NCT04252027 Completed - Clinical trials for Critically Ill Patients

Therapeutic Drug Monitoring of Fluconazole in Critically Ill Patients

Start date: April 23, 2019
Phase:
Study type: Observational

This prospective study will research the exposure and its variability to fluconazole after longitudinal administration in critically ill patients

NCT ID: NCT04045366 Recruiting - Clinical trials for Critically Ill Patients

Impact of Capillary Leak and Hypoalbuminemia on PK/PD of Anidulafungin and Caspofungin in Critically Ill Patients

Start date: September 21, 2012
Phase:
Study type: Observational

This prospective study will explore the pharmacokinetic exposure and pharmacodynamics of the echinocandins (caspofungin or anidulafungin) in critically ill patients.

NCT ID: NCT03698292 Recruiting - Clinical trials for Critically-ill Patients

Itopride in Feeding Intolerance of Critically-ill Patients Receiving Enteral Nutrition

Start date: October 2018
Phase: N/A
Study type: Interventional

The current study will compare the effectiveness as well as the safety of Itopride against metoclopramide as the first line treatment for feeding intolerance in critically ill patients.

NCT ID: NCT03529617 Recruiting - Pharmacokinetics Clinical Trials

Pharmacokinetics of Liposomal Amphotericin B in Critically Ill vs. Non-critically Ill Hematological Patients: Exploration of Covariates

Start date: October 19, 2016
Phase:
Study type: Observational [Patient Registry]

This prospective study will compare the pharmacokinetic exposure to liposomal amphotericin B between critically ill patients and non-critically ill (hematology) patients in an early and late exposure day.

NCT ID: NCT03469882 Completed - Clinical trials for Critically Ill Patients

High Protein Intake and Early Exercise in Adult Intensive Care Patients

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

This study analyse the impact of high protein intake associated to early programed exercise on functional outcomes of adult intensive care patients.

NCT ID: NCT03354260 Terminated - Nutrition Clinical Trials

Optimization of Oral Diet in Critically Ill Patients

NAP-REA
Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The purpose of the present study is to evaluate the effects of a personalized oral diet in the critically ill patients during ICU stay and after as compared usual oral diet.

NCT ID: NCT03205592 Completed - Clinical trials for Critically Ill Patients

Ultrasound Assessment of Residual Gastric Content in Critically Ill Patients

GastrICU
Start date: July 3, 2017
Phase:
Study type: Observational

This prospective observational study aims to assess whether ultrasound assessment of gastric content may be useful for the monitoring of the gastric residual content in critically ill patients