Feasibility and Initial Clinical Impressions of Predictive Monitoring Integrated With the RACE Team
Recruiting
N/A
Interventional Study
Deterioration, Clinical
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 140 (estimated)
- Sponsor
- Ottawa Hospital Research Institute · Other
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About This Trial
Rapid response teams (RRTs) have been adopted by hospitals to provide urgent critical care to hospitalized patients who require quick intervention to prevent further deterioration. Early warning scores (EWS) serve as a method to identify patients requiring RRT assessment by analyzing routinely collected data such as vital signs and laboratory results. The Visensia Safety Index (VSI) is an EWS that…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Adult patient (greater than or equal to 18 years of age) designated for the most aggressive levels of potential intervention (Category 1 status - Full Care and Category 2 status - Full Care except CPR) who belong to one of the following groups:
* Patients who have undergone hig…
Contacts