Clinical trials: Intensive Care Patients
Critical Care, Intensive Care
Physiologic Signals and Signatures With the Accuryn™ Monitoring System in Intensive Care Patients
The purpose of the study is to collect physiologic data streams with the Accuryn Monitoring System and validate the accuracy of these measurements against existing gold standards, and to track and analyze changes in these…
- Trial name
- PRESCIENT (NCT02602782)
- Volunteers
- 76 people
- Sponsor
- Potrero Medical
Surgery, Intensive Care Units
Study to Compare CAUTI Rates Following ERASE CAUTI Tray Non-Silver vs Silver Coated Foley Catheters
The Foley catheter is one component in a catheter insertion procedure that could contribute to a catheter associated urinary tract infection (CAUTI).
- Trial name
- NCT02101762
- Volunteers
- 756 people
- Sponsor
- Medline Industries
Neonatal Intensive Care
Estimation of Cardiac Output in Neonatal ICU Using an Ultrasound Dilution Technique
Presently there is no apparatus, clinically available, for routine determination of cardiac output (CO) in children. The goal of this research is to develop new technology that will help determine CO in neonates.
- Trial name
- CH (NCT01610622)
- Testing
- COstatus cardiac output measurement with isotonic saline
- Where
- United States
- Volunteers
- 7 people
- Sponsor
- Transonic Systems Inc.
Intensive Care
Measurement of Cardiac Output and Intravascular Volume Status in Children Using COstatus (SH)
Assessment and monitoring of cardiac function in the pediatric intensive care unit (PICU) is an integral part of hemodynamic monitoring of critically ill patients whether it is done directly or indirectly.
- Trial name
- NCT01613859
- Where
- United States
- Volunteers
- 9 people
- Sponsor
- Transonic Systems Inc.
Intensive Care Unit Blood Glucose Monitoring
GlucoClear ICU Study
The primary purpose of this Study is evaluation of the safety and accuracy of the GlucoClear CGM System.
- Trial name
- NCT02238041
- Testing
- GlucoClear System
- Sponsor
- Edwards Lifesciences
Intensive Care Unit
Study to Evaluate Hemodynamic Effect of Different Loading Doses of Precedex in Post-surgical Intensive Care Unit (ICU) Patients
The objective of this study is to characterize the hemodynamic effects of Precedex (dexmedetomidine (DEX)) during 3 loading-dose paradigms in mechanically ventilated post-surgical subjects in an intensive care setting.
- Trial name
- NCT01169571
- Testing
- Dexmedetomidine
- Where
- 17 sites in Canada
- Volunteers
- 373 people
- Sponsor
- Hospira, now a wholly owned subsidiary of Pfizer
Adult Intensive Care Patients
GlySure Acute Care Settings Study
The company who have developed the GlySure product have previously carried out a study to be able to show that the GlySure system is accurate in measuring blood sugar (glucose) levels.
- Trial name
- NCT02421107
- Testing
- Glysure CGM, iStat intermittent testing
- Volunteers
- 40 people
- Sponsor
- GlySure
Intensive Care Patients
Blood Glucose Control in Intensive Care Patients Using the Space GlucoseControl System
Glucose metabolism is impaired in many critically ill patients and is often aggravated by parenteral feeding, infections and/or pre-existent diabetes.Therefore insulin infusion protocols, which are based on frequent bedside…
- Trial name
- NCT01523665
- Where
- 17 sites in Czechia, Denmark and 7 more
- Volunteers
- 508 people
- Sponsor
- B. Braun Melsungen AG
Immobility and Weakness Associated With Long Intensive Care Unit Stays
Early Progressive Mobility in the CVICU: Assessing Current Status
The current study is proposed to assess the frequency and type of progressive mobility procedures currently performed in the CVICU The study will evaluate the type and frequency of progressive mobility orders, whether or not…
- Trial name
- NCT01295541
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- Hill-Rom
Critical Care, Mechanical Ventilation
Investigating Modes of Progressive Mobility
The purpose of this study is to compare the effects of specific activities with and without an early therapeutic mobility (ETM) protocol among patients who experience three or more days of mechanical ventilation.
- Conditions
- Critical Care, Mechanical Ventilation, Intensive Care, Muscular Atrophy
- Trial name
- NCT00787098
- Testing
- ETM protocol
- Volunteers
- 82 people
- Sponsor
- Hill-Rom