An observational study in Kidney Injury, sponsored by Intermountain Health Care, Inc.. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-02-12.
Sponsored by Intermountain Health Care, Inc. · Observational
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.
Intermountain Health Care, Inc. is the lead sponsor of 118 studies on the registry; 15 are open to participants now.
Of its 9 completed or terminated interventional studies of FDA-regulated products, 3 (33%) have results posted.
Counted across the registry records on this site, refreshed daily.
Data to determine study outcomes will be extracted from the EDW and stored in a secure database. No actualy contact with patients will take place for this data-only study
Exclusion Criteria:
Patients in this group will be included in the project
Number of participants with major Adverse Kidney Events
death from any cause, new renal replacement therapy or persistent renal dysfunction
Time frame: within 30 days or at hospital discharge
LR IV Fluids administered
Proportion of LR IV fluids following implementation
Time frame: Through study completion (an average of 1 year)
Rate of hospital admission and readmission
Time frame: Within 30 days of initial ED encounter
Cost
Direct costs of ED care and hospitalization
Time frame: Through study completion (an average of 1 year)
Plan to share: No
No publications or documents are linked to this record.
This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.
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Intermountain Health Care, Inc.