Wireless Monitoring for Clinical Deterioration
ConditionInpatient Facililty Diagnoses
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14+
SponsorKing Abdullah International Medical Research Center
About this trial
The study evaluates whether implementing a wireless monitoring system for patients admitted to hospital wards reduces mortality and cardiopulmonary failure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 14 years or older
Checked in as inpatient status to one of the study wards
Disqualifiers
Cardiology, pediatric, obstetric wards
ICUs and emergency departments
Operating rooms
Outpatient clinics
Trial design
Design model
Sequential
Treatments tested in this trial
wireless monitoring
DeviceThe monitoring wireless system will continuously monitor the heart rate, oxygen saturation (SpO2), respiratory rate, and blood pressure and in selected patients electrocardiography (ECG).
Treatment groups
13,160 Participants
are divided into 2 treatment groupsGroup A: Wireless monitoringActive comparator 0 interventions
Group B: ControlNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Composite endpoint of 30-day in-hospital mortality, cardiac arrest, requirement of vasopressor or intubation
After hospital admission within 30 days
Time frame
30 daysSecondary outcomes
1
Cardiac arrest
cardiac arrest within 30 days of hospital admission
Time frame
30 days2
Requirement of vasopressors
use of vasopressors/inotropic support
Time frame
within 30 days of hospital admission3
Requirement of intubation
need for mechanical ventilation within 30 days of hospital admission
Time frame
30 days4
Hospital length of stay
censored at 90 days
Time frame
90 daysSponsors and contacts
Click on the lead sponsor to view all of their trials.
King Abdullah International Medical Research Center
Lead sponsor
King Saud Bin Abdulaziz University for Health Sciences
Sponsor institution
Source ClinicalTrials.gov