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Intensive Care Units clinical trials

View clinical trials related to Intensive Care Units.

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NCT ID: NCT02267174 Completed - Communication Clinical Trials

Handoffs and Transitions in Critical Care

HATRICC
Start date: July 2014
Phase: N/A
Study type: Interventional

The HATRICC study will use mixed methods to implement a standardized process for operating room to intensive care unit handoffs that is accepted and sustainably used by perioperative clinicians.

NCT ID: NCT02040051 Completed - Clinical trials for Intensive Care Units

Efficacy of Sound Insulation and Music Therapy on the Comfort of Mechanically Ventilated Patients Admitted to Intensive Care Unit

Start date: June 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of sound insulation and music therapy on the comfort of mechanically ventilated patients admitted to intensive care unit measured by the Bispectral Index (BIS), the Ramsay sedation scale and the Behaviour Pain Scale (BPS)

NCT ID: NCT01235637 Completed - Pediatric Clinical Trials

Alfentanil Versus Sufentanil for Pain in Children During for Tracheal Suction

DOLOREAPEDIA
Start date: June 2010
Phase: Phase 3
Study type: Interventional

The main objective is to assess the efficacy of Alfentanil for pain in children treated by tracheal suction in pediatric intensive care units in France, compared to Sufentanyl, the current standard treatment.

NCT ID: NCT00893672 Completed - Clinical trials for Intensive Care Units

Comparison of Two Chest Radiograph Prescription Strategies in Intensive Care Unit

RARE
Start date: December 2006
Phase: N/A
Study type: Observational

Current guidelines recommend Routine daily chest radiographs (CXRs) for mechanically ventilated patients in intensive care units (ICUs). However, some ICUs have shifted to an On-demand strategy, in which this CXR is only prescribed if warranted by the patient's status at the morning physical examination. Here the investigators compared Routine and On-demand strategies in 21 French ICUs. The working hypothesis was that CXR prescriptions would fall by at least 20% with the On-demand strategy, with no reduction in quality of care.

NCT ID: NCT00466492 Completed - Critical Illness Clinical Trials

Advantages and Disadvantages of Long Term Sedation in Intensive Care Unit Patients

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether sedation of the critical ill patient prolongs the time receiving mechanical ventilation.

NCT ID: NCT00461461 Completed - Clinical trials for Intensive Care Units

a Multifaceted Program for Improving Quality of Care in ICU

Start date: January 2007
Phase: N/A
Study type: Interventional

Medical errors that affect patient safety have generated huge concern since the publication of "To Err Is Human" 6 years ago [1]. Given the complexity of management in the intensive care unit (ICU) and the nature of human activities, critically ill patients are exposed to adverse events (AEs) induced by medical errors. A large number of studies have focused on AEs and medical errors in ICUs [2-6], one of their main goals being to identify strategies for preventing AEs and thereby improving patient outcomes. Choosing the best AE to serve as an indicator for the risk of medical error is challenging. In 2005, our group conducted a systematic literature review and presented the results to 30 national experts with clinical backgrounds in internal, emergency, and intensive care medicine. Using the Delphi technique, these experts selected 14 AEs that had the following characteristics: high frequency, easy and reproducible definition, association with morbidity and mortality, and ease of reporting without fear of punishment (Iatroref I study) (ref abstract). These AEs were used in a French multicenter study (75 ICUs) for a weeklong incidence evaluation (Iatroref II study) (ref abstract). Preliminary evaluation of the results allowed us to choose the following AEs for the current Iatroref III study: error in insulin administration, error in anticoagulant administration, error in anticoagulant prescription, unplanned extubation, and unplanned removal of central venous catheter. Evidence suggests that guidelines alone without reinforcing strategies may be insufficient to change provider behavior and that the most effective interventions may be multifaceted rather than single-component strategies ([7]). This study will test a composite intervention program. The objectives of the study are to determine whether the introduction of a composite intervention program decreases the predefined AEs. Study hypothesis: The intervention program will decrease the incidence of the predefined AEs.