Intermountain Medical Center
Murray, Utah, 84157-7000, United States
NCT Number: NCT03807648
To study the difference in mortality and major adverse kidney events during and after treatment in the emergency department with intravenous fluids per standard of care at 30 days before and after the system-wide implementation.
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Notify Me18 year and older
All sexes
Observational
Murray, Utah, 84157-7000, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients in this group will be included in the project
Time frame: within 30 days or at hospital discharge
death from any cause, new renal replacement therapy or persistent renal dysfunction
Time frame: Through study completion (an average of 1 year)
Proportion of LR IV fluids following implementation
Time frame: Within 30 days of initial ED encounter
Time frame: Through study completion (an average of 1 year)
Direct costs of ED care and hospitalization
Intermountain Health Care, Inc.
Other
Intermountain Utah Study Evaluating the Implementation of Lactated Ringers as Standard Resuscitation Fluid Starting in Emergency Department
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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