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Intensive Care Unit clinical trials

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NCT ID: NCT03831035 Completed - Intensive Care Unit Clinical Trials

Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit

REUNIR
Start date: April 8, 2019
Phase:
Study type: Observational

An early diagnosis of congenital malformations and suspected genetic conditions in critically ill infants is essential to perform specific adapted care, prevention, and give proper genetic counseling. However, etiologies are various and each of them is individually very rare. Thanks to next-generation sequencing technologies, diagnosis time frames have drastically decreased and the investigators have observed an increase in diagnosis yields. This study aims to evaluate the feasibility of fast trio exome sequencing (less than 16 days between informed consent signature and the consultation for results to the parents) in infants under the age of 12 months hospitalized in Intensive Care Unit (ICU).

NCT ID: NCT03789305 Completed - Critical Illness Clinical Trials

Differences in Frail and Non-frail Critically-ill Patients in Functional Outcomes

DEFAULT
Start date: April 1, 2017
Phase:
Study type: Observational

This is a prospective analysis of patient registry data of intensive care patients. The aim is to investigate if frailty is a predictor of decline of functional status of critically ill patients during their hospital stay.

NCT ID: NCT03681626 Completed - Critically Ill Clinical Trials

Does Tracheal Suction During Extubation in Intensive Care Unit Decrease Functional Residual Capacity

Start date: October 27, 2015
Phase: N/A
Study type: Interventional

Little is known about the procedure of extubation of patients admitted in Intensive Care Units (ICU). In particular, effects of tracheal suction during extubation have never been evaluated. Tracheal suction induces alveolar derecruitment in sedated patients under mechanical ventilation and is a major source of pain. The aim of this study was to evaluate the impact of tracheal suction during the extubation procedure of critically ill patients on the end-expiratory lung volume.

NCT ID: NCT03680274 Completed - COVID-19 Clinical Trials

Lessening Organ Dysfunction With VITamin C

LOVIT
Start date: November 8, 2018
Phase: Phase 3
Study type: Interventional

LOVIT is a multicentre concealed-allocation parallel-group blinded randomized controlled trial to ascertain the effect of high-dose intravenous vitamin C compared to placebo on mortality or persistent organ dysfunction at 28 days in septic intensive care unit patients. Patients with COVID-19 are considered eligible for this study.

NCT ID: NCT03634943 Completed - Critical Illness Clinical Trials

Evaluation of Nutritional Practices in the Critical Care

ENPIC
Start date: April 23, 2018
Phase:
Study type: Observational

Background: The adequacy of the artificial Nutritional Support (NS) in the critical care patient has implications in morbidity and prognosis. Clinical practice guidelines (CPG) are an important tool for healthcare professionals in their daily practice and a method of consultation for the correct treatment of patients. Also, the evidence remains low and there are important controversies regarding the NS in the critical care patient. Hypothesis: The NS generates great controversy in the professionals involved in the care of critical care patients due to the contradictory results in literature. Despite this, the CPG should serve to standardize the treatment of patients and provide a better adherence to current knowledge in this setting. The importance of NS is underestimated and there is a need to perform proper evaluation of the impact of nutrition. Objectives: To evaluate and analyze NS practices in critically ill patients in different ICUs and assess the adherence to CPGs. To evaluate the relationship of nutrition and outcomes in the ICU. Methodology: Prospective multicenter observational study. Collection of variables from different participating ICUs and the characteristics of the NS of the different admitted patients. Monitoring of nutritional practices and complications. Evaluation of outcomes (e.g. mortality, ICU complications, etc.) with NS. Expected results: Better understanding of the NS and its impact on morbidity and mortality; development of strategies to reduce low adherence to CPGs, improving the quality of care associated with this field in critical care patients; obtain clinical information that will serve as a basis for conducting intervention studies.

NCT ID: NCT03588637 Completed - Intensive Care Unit Clinical Trials

Real-world Daptomycin Use in Chinese ICUs

Start date: June 1, 2018
Phase:
Study type: Observational [Patient Registry]

Analyze the effectiveness and safety of Daptomycin(Jiangsu Hengrui Medicine Co., Ltd) in Gram-positive infections in Chinese Intensive Care Units by using the real-world data platform, https://rws.scccmqc.com. Patients who received at least one dose of Daptomycin between 2016 to 2021 are eligible.

NCT ID: NCT03535441 Completed - Intensive Care Unit Clinical Trials

HMGB1 Release From Hemorrhagic Shock Patients

Start date: May 17, 2017
Phase:
Study type: Observational

It is reported that high mobility group box 1 (HMGB1), a non-histone nuclear protein, can serve as an alarmin with damage associated molecular patterns to activate immune responses in the early stages of hemorrhagic shock (HS). However, the origin of HMGB1 and how it is released following HS is poorly understood. In this study, we teased out this mechanism. We try to record the concentration of serum HMGB1 protein following HS in clinical patients.

NCT ID: NCT03520023 Completed - Palliative Care Clinical Trials

Critical Care and Palliative Care Medicine Together in the ICU

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

Will earlier palliative care medicine consultation in the ICU result in decreased length of stay in the ICU and hospital, as well as, increased patient and family satisfaction. Secondary questions to be answered is if this early consultation changes ICU and hospital death, discharge destinations, hospice admissions, code status changes, and withdrawal of life sustaining interventions.

NCT ID: NCT03430817 Completed - Intensive Care Unit Clinical Trials

Citicholine-Amantadine Trial in Traumatic Brain Injury

Start date: December 7, 2017
Phase: Phase 4
Study type: Interventional

This randomized study aims at comparing between the effects of amantadine, citcholine and its combinations on arousal and behavioral consequences in early phase of moderate Traumatic Brain injury (TBI).

NCT ID: NCT03131063 Completed - Sepsis Clinical Trials

Pharmacokinetic Study of Antibiotics in Patients Assisted by Extracorporeal Membrane Oxygenation (PHARMECMO)

PHARMECMO
Start date: May 2014
Phase: N/A
Study type: Observational

The PHARMECMO study is a pilot, prospective, pharmacokinetic study, conducted in a cardiac surgery intensive care unit of 18 beds. Optimization of antibiotic therapy for extracorporeal membrane oxygenation (ECMO) patients remains a pharmacological challenge. Clinical studies suggest that individualized dosing strategies and therapeutic drug monitoring could facilitate the achievement of adequate antibiotic concentration. The objective of this pilot study was to observe the pharmacokinetic characteristics of commonly used antibiotics in intensive care for patients treated with extracorporeal membrane oxygenation.