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Continuous Ward Monitoring With the GE Portrait Mobile Monitoring Solution: the COSMOS Trial — COSMOS  

Postoperative Complications Clinical Trial

Official title:
Continuous Ward Monitoring With the GE Portrait Mobile Monitoring Solution: the COSMOS Trial

Clinical Trial Summary

The investigators plan to determine whether unblinded continuous ward monitoring with the GE Portrait Mobile Monitoring Solution and nursing alerts reduces vital sign abnormalities in patients recovering from major noncardiac surgery.

Clinical Trial Description

Primary Aim. Determine whether unblinded continuous ward monitoring with the GE Portrait Mobile Monitoring Solution and nursing alerts reduces vital sign abnormalities in patients recovering from major noncardiac surgery. Primary hypothesis. Unblinded continuous ward monitoring and nurse alerts reduces vital sign abnormalities during the initial 48 postoperative hours after major non-cardiac surgery while patients remain hospitalized. Secondary Aim. Determine whether continuous ward saturation, ventilation, and pulse rate monitoring reduces a composite of substantive respiratory and cardiovascular interventions. Secondary hypothesis. Unblinded continuous ward monitoring increases a composite of clinical interventions for desaturation, hypoventilation, tachypnea, tachycardia, and bradycardia within 48 hours after major non-cardiac surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06133140
Study type Observational
Source The Cleveland Clinic
Contact Daniel I Sessler, MD
Phone 216-445-6500?
Email sessled@ccf.org
Status Recruiting
Phase
Start date February 14, 2024
Completion date June 1, 2026
View Details
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