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Critical Care clinical trials

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NCT ID: NCT03092297 Terminated - Anemia Clinical Trials

Insufficient Cellular Oxygen in ICU Patients With Anaemia

INOX ICU-2
Start date: May 16, 2017
Phase:
Study type: Observational

The purpose of this study is whether the mitochondrial oxygenation tension (mitoPO2) is a feasible and reliable tool in ICU patients with anaemia undergoing red cell transfusion to ultimately personalize blood transfusion decisions in the ICU.

NCT ID: NCT03090867 Active, not recruiting - Critical Care Clinical Trials

Participation of Relative or Surrogate in the Patient's Care in Reanimation

PARTICIPATE
Start date: November 16, 2017
Phase: N/A
Study type: Interventional

ICUs have always perceived by the public has a very technical unit with a restricted and/or forbidden access. Physical alteration of the patient, seeing the patient sedated, the large numbers of devices, the alarms and an uncertain prognosis. All this factors can be perceived by people close to the patient as a source of stress. In the literature, numerous studies have shown that families develop anxiety and depression symptoms while their loved one is hospitalized in the ICU. French intensive care societies thought of ways to prevent or diminish these symptoms. The 6th consensus conference on " Live better in the ICU " recommends: effective and adapted information, large visiting hours to reach an unrestricted access and family participation in care. The unit has taken this path to improve patient and family centered care by: creating a welcome leaflet, a room dedicated to meetings with families and an ICU open 24/7bto families, with the possibility for children to visit their parents. Hence, spontaneously, relatives have expressed the wish to participate to certain care and when participating, expressed their satisfaction. This observation and testimonies from family members and patients led us to think about the impact of participation of care. Two major French studies have shown contradictory outcomes: 16% of families would have been willing to participate in the first study against 97% in the second one. These studies were survey done after the ICU discharge. No study today has assessed the actual impact of family participation in care. The aim of this clinical trial is to diminish anxiety and depression symptoms. By participating in care, relatives can develop or strengthen a relationship of trust with caregivers. It could contribute also to a better understanding of the plan of care and an easier context to announce negative outcomes.

NCT ID: NCT03041974 Completed - Critical Care Clinical Trials

Impact of Microparticles in Blood on Transfused Patient Outcomes

IMIB
Start date: March 2011
Phase: N/A
Study type: Observational

During storage, red blood cells (RBCs) undergo changes collectively termed "Storage lesions". these changes may have an impact of the outcomes of transfused patients. One of these changes is the release of microparticles by RBCs and other blood cells types. The aim of the study is to (1) quantify red cell- and platelet-derived microparticles in RBC concentrates, and (2) evaluate the impact of transfused microparticles (MPs) on survival and post-transfusion complications in critical care patients participating in the ABLE trial (ISRCTN44878718).

NCT ID: NCT03040570 Completed - Hypoxia Clinical Trials

Conservative Versus Liberal Oxygenation Targets in Critically Ill Children

Oxy-PICU
Start date: March 4, 2017
Phase: N/A
Study type: Interventional

A feasibility study to determine if it is possible to perform a safe, adequately powered, and affordable multi-centre study in critically ill children comparing current practice of liberal targets for systemic oxygen levels with more conservative targets.

NCT ID: NCT03011853 Completed - Critical Care Clinical Trials

Survival After Failed First-line Non-invasive Ventilation in Acute on Chronic Obstructive Pulmonary Disease

Start date: January 2008
Phase:
Study type: Observational [Patient Registry]

Observational cohort study of mid-to-long term survival of patients with acute on chronic obstructive pulmonary disease, analyzed per type of ventilation support provided during first 24 hours in intensive care.

NCT ID: NCT02970903 Withdrawn - Critical Care Clinical Trials

VitalPAD: an Intelligent Monitoring and Communication Device to Optimize Safety in the PICU

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

The VitalPAD is a unified, portable and intelligent device that integrates information from multiple patient monitors, mechanical ventilators, infusion pumps and clinical information systems on a mobile platform. It will allow nurses, respiratory therapists and physicians to continuously monitor and coordinate care of critically ill patients. This study will use a participatory design process to guide the design of an integrated mobile device, followed by an evaluation of the proposed device in a simulated ICU setting.

NCT ID: NCT02963558 Completed - Critical Illness Clinical Trials

A Study Promoting Critical Illness Recovery in the Elderly

ASPIRE
Start date: May 30, 2017
Phase: N/A
Study type: Interventional

This proposal will test the hypothesis that EARLY application of a novel early rehabilitation therapy in critically ill patients will improve functional outcomes, and change the functional trajectory of this population. A pilot study of early mobilization with a cycle ergometer will be performed and translate into humans the pre-clinical mechanisms that may mediate the effects of early mobility. A second phase of the study was added in September 2019, which will focus on clinical outcomes.

NCT ID: NCT02952846 Completed - Child Clinical Trials

Tapering of Analgosedation and Occurrence of Withdrawal Syndrome in Paediatric Intensive Care Treatment

ASWISPIC
Start date: May 2016
Phase: N/A
Study type: Interventional

The study is a prospective interventional study with three main aims: 1. Describe the frequency and severity of withdrawal syndrome in a population of paediatric intensive care patients. 2. Test whether implementation of an algorithm for tapering of analgosedation changes the frequency and severity of withdrawal symptoms in the same population. 3. Investigate how the health care providers experience having to adhere to such an algorithm.

NCT ID: NCT02922101 Completed - Pain Management Clinical Trials

Evaluation of the Effectiveness of an Audit and Feedback Intervention With Quality Improvement Toolbox in Intensive Care

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

This study evaluates the addition of a quality improvement toolbox to an online audit and feedback intervention in Dutch intensive care units. The toolbox comprises for each quality indicator (e.g., percentage of patients per shift whose pain is measured) a list of potential bottlenecks in the care process (e.g., staff is unaware of the prevailing guidelines for measuring pain every shift), associated recommendations for actions to solve mentioned bottlenecks (e.g., organize an educational training session), and supporting materials to facilitate implementation of the actions (e.g., a slide show presentation discussing the importance and relevance of measuring pain every shift). Half of the participating intensive care units will only receive online feedback, while the other half will additionally gain access to the integrated toolbox to facilitate planning and executing actions.

NCT ID: NCT02902783 Completed - Critical Care Clinical Trials

DONATE-Pilot Study on ICU Management of Deceased Organ Donors

DONATE-Pilot
Start date: September 2015
Phase:
Study type: Observational [Patient Registry]

The DONATE-Pilot is a prospective observational cohort study in organ donation (OD) that observes the ICU management of consented deceased organ donors at 4 high volume centres over a period of 12 months each. The pilot study will be followed by a 1-year prospective national observational study a 15-20 ICUs across Canada.