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Intensive Care Unit Syndrome clinical trials

View clinical trials related to Intensive Care Unit Syndrome.

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NCT ID: NCT03172897 Suspended - Delirium Clinical Trials

Low-dose Dexmedetomidine in Mechanically Ventilated ICU Patients

Start date: August 20, 2017
Phase: Phase 4
Study type: Interventional

For patients undergoing mechanical ventilation, light sedation is better than deep sedation for the outcomes, which is manifested as shortened length of ICU stay, shortened duration of mechanical ventilation, and decreased mortality. In a recent study of the investigators, low-dose dexmedetomidine without sedative effects (0.1 ug/kg/h) improved sleep quality and reduced the incidence of delirium in elderly patients admitted to the ICU after surgery. The investigators hypothesize that, for ICU patients with prolonged mechanical ventilation, low-dose dexmedetomidine infusion (0.1 ug/kg/h) may also be effective in decreasing delirium. The purpose of this study is to investigate whether low-dose dexmedetomidine infusion can reduce the incidence of delirium in ICU patients with prolonged duration of mechanical ventilation (>= 24 hours).

NCT ID: NCT03138278 Withdrawn - PTSD Clinical Trials

Impact on Family or Care-givers of Very Old ICU-survivors, Trajectories and 6 Months' Outcome in the Very Old.

VIP2
Start date: May 2023
Phase: N/A
Study type: Interventional

It is known from extensive documentation that second victims in critical illness often are the care givers of the patients: family, friends or other persons. Although this has not been specifically studied in the very old patients, there is no reason to believe that this group will be different from other ICU patients. Even more so, in this very old age patient group there are seldom any older relatives. Partners, like wife/husband or other cohabitants, may be dead or themselves incapacitated. Many will be in institutional care. The closest care-givers will be middle-aged people such as children or others, if no partners are available. The hypothesis is that critical illness can be a large stressor to care-givers of survivors in the VIP measured as the occurrence and severity of the usual problems like PTSD and depression. The investigators hypothesize that a low-threshold on-line support program decreases the magnitude of anxiety, depression and PTSD for care-givers of very old intensive care patients (VIP) after discharge.

NCT ID: NCT03124342 Completed - Clinical trials for Intensive Care Unit Syndrome

Vanderbilt ICU Recovery Program Pilot Trial

VIP
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Every year, millions of Americans are admitted to the intensive care unit. Due to advances in critical care, mortality rates are decreasing, increasing the number of ICU survivors. Survivors of critical illness, however, often face physical, functional, and cognitive deficits that place them at risk for a cycle of re-hospitalization that frequently culminates in premature death. Moreover, post-ICU interventions may be resource-intensive and may be most cost-effective only in a subgroup of patients at highest risk. Whether a multi-disciplinary program to facilitate recovery from critical illness can prevent hospital readmission and improve quality of life among high-risk ICU survivors remains unknown. The primary aim of this pilot is to examine the feasibility of implementing a multidisciplinary ICU Recovery Program and the influence of such a program on process measures including contact with the ICU recovery team and attendance of ICU recovery clinic. The secondary aims are to compare the effect of an ICU Recovery Program on 30-day same-hospital readmission and other clinical outcomes.

NCT ID: NCT03055169 Completed - Hyperglycemia Clinical Trials

TCF7L2 Polymorphisms Influence on Glycemic Control in ICU Patients With Organ Failure

READIAB-G4
Start date: April 2012
Phase:
Study type: Observational

This study evaluates the link between genetic polymorphisms as r7903146, rs12255372 of TCF7L2 gene and the risk of developing hyperglycemia during Intensive care unit stay

NCT ID: NCT03050021 Completed - Delirium Clinical Trials

Risk Factors for Delirium in Critically Ill Surgical Patients

Start date: April 1, 2013
Phase: N/A
Study type: Observational

Delirium is characterized by changes in mental status, inattension, disorganized thinking, and altered consciousness. Prevalence of delirium in critically ill patients has varied from 20~80% depending on the severity of illness. Despite its high prevalence, delirium is often under-recognized by clinicians due to the difficulties in diagnosis and no interest. Delirium is associated with increased mechanical ventilation days, hospital length of stay, and mortality. The purpose of this study is to analyze the prevalence of delirium and risk factors for delirium in critically ill surgical patients.

NCT ID: NCT03023839 Completed - Delirium Clinical Trials

Incidence and Risk Factors for Delirium in Severely Injured Patients

Start date: February 2015
Phase: N/A
Study type: Observational

Delirium is very common in intensive care unit (ICU) patients and leads to poor outcomes. There is little information on delirium in injured patients however. This study determined the incidence and risk factors for delirium in severely injured patients.

NCT ID: NCT02919085 Completed - Muscle Weakness Clinical Trials

Effect of Critical Patients Mobilization on Respiratory and Peripheral Muscle Strength and Functional Capacity.

Start date: December 2016
Phase: N/A
Study type: Interventional

To analyze changes on respiratory muscle strength, peripheral and functional capacity of critically ill patients with clinical and surgical etiology, breathing spontaneously and bedridden, within 48 hours of admission to the intensive care unit (ICU) and if there are correlations among these variables. This is an observational study. Respiratory muscle strength will be assessed through the maximum inspiratory pressure (MIP) and maximal expiratory pressure (MEP) and peripheral muscle strength, by the Medical Research Council score (MRC) and hand grip test and functional capacity through the Functional Independence Measure (FIM) and Physical Function ICU Test Score (PFIT-s) in the period between 24h and 48h of hospitalization in the adult ICU. For descriptive purposes, the sample will be stratified according to clinical and surgical characteristics. Correlations will be determined using the Pearson test, with significance level of p <0.05.

NCT ID: NCT02849756 Completed - Clinical trials for Intensive Care Unit Syndrome

Future of the Older Patients After Intensive Care Unit

DAAR
Start date: February 2015
Phase:
Study type: Observational

Estimate the future six months after the admission in an intensive care unit of the patients of 85 and more years old in terms of autonomy.

NCT ID: NCT02784574 Completed - Critical Illness Clinical Trials

Post ICU Follow up: A Questionnaire Survey of Aftercare in Denmark

Start date: May 2016
Phase: N/A
Study type: Observational

This study aims to investigate current aftercare activities in Denmark after intensive care unit (ICU) treatment. The hypothesis is that a large number of hospitals offer aftercare, and these interventions are heterogenic and differ between hospitals and regions. This study is an electronic questionnaire survey that aim to describe and map Danish aftercare activities, and future development plans in this field.

NCT ID: NCT02767180 Completed - Clinical trials for Intensive Care Unit Syndrome

Evaluation of an ICU-specific Questionnaire for Patient-reported Outcome Measures

Start date: April 2016
Phase:
Study type: Observational

An ICU-specific questionnaire for patient reported outcome measures (PROM) after critical care will be tested in a study of 650 patients recruited six months to three years after discharge from the ICU, and 150 controls who have not been critically ill, matched for age and sex. The questionnaire is sent by mail after an invitation letter followed by a phone call and returned in a pre-stamped envelope. It is then scanned and data imported digitally. Medical data from the ICU-stay can be added. Further analyses after comparison with the control population and item reduction will follow.