CompletedNot Applicable

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

United States227 participantsStarted 2024-02-14

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Are expected to be admitted to one of the wards equipped with the GE Portrait Mobile Monitoring Solution;
✓. Are ≥18 years old;
✓. Are designated American Society of Anesthesiologists physical status 1-4;
✓. Are scheduled for major noncardiac surgery lasting at least 1.5 hours;
✓. Are expected to remain hospitalized at least one postoperative night;
✓. Are expected to have general or neuraxial anesthesia.

Exclusion criteria

✕. Have language, vision, or hearing impairments that might compromise continuous monitoring;
✕. Are designated Do Not Resuscitate, hospice, or receiving end of life care;
✕. Are expected to have telemetry monitoring;
✕. Have previously participated in the study.

What they're measuring

Hypoxemia

Timeframe: 48 postoperative hours.

Inadequate or excessive ventilation

Timeframe: 48 postoperative hours.

Bradycardia and tachycardia

Timeframe: 48 postoperative hours.

Trial details

NCT IDNCT06133140

SponsorThe Cleveland Clinic

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-01-01

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