The purpose of this study is to evaluate overall changes in patient management and longer-term resource utilization between control and test arms, including (but not limited to) additional work-up (including other diagnostic tests and consults), antimicrobial treatments, disposition decisions and hospital length of stay (LOS)
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Cost of any additional diagnostic tests done by a participant
Timeframe: from day of admission to emergency department upto about 28 day follow up
Cost of any additional consults done by a participant
Timeframe: from day of day of admission to emergency department upto about 28 day follow up
Total cost of any antimicrobial treatments by a participant
Timeframe: end of study (about 28 days from baseline)
Number of participants that were admitted to the hospital
Timeframe: end of study (about 28 days from baseline)
Cost of hospital stay
Timeframe: end of study (about 28 days from baseline)
Length of hospital stay
Timeframe: at time of discharge( from 28 days- 6months from baseline)