Prospective Cohort Study of Rapid Response Team
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15+
SponsorSeoul National University Hospital
About this trial
The purpose of this study is to collect data of rapid response team activated patients prospectively
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
patients admitted to pediatric wards
patients in emergency room, intensive care unit, and operating room
Trial population
Patients admitted to general ward in Seoul National University Bundang Hospital and monitored by in-hospital rapid response system.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
mortality or ICU admission of rapid response team activated patient
Time frame
an average of 1 year2
incidence of preventable cardiac arrest
Time frame
an average of 1 yearSecondary outcomes
1
Frequency of triggerring criteria(1) for activation of rapid response team
SBP \<90mmHg(mABP 60mmHg) +- clinically correlated symptom or sign
Time frame
an average of 1 year2
Frequency of triggerring criteria(2) for activation of rapid response team
HR: \<50/min or \>140/min or symptomatic arrythmia
Time frame
an average of 1 year3
Frequency of triggerring criteria(3) for activation of rapid response team
RR: \<10/min or \>30/min or stridor(sign of airway obstruction) or accessary muscle use
Time frame
an average of 1 year4
Frequency of triggerring criteria(4) for activation of rapid response team
Oxygenation: SaO2 \<90% in room air or FM 8L/min
Time frame
an average of 1 yearSponsors and contacts
Click on the lead sponsor to view all of their trials.
Seoul National University Hospital
Lead sponsor
Seoul National University Bundang Hospital
Collaborator
Source ClinicalTrials.gov