COMPLETED

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

Conditions

Postoperative Complications Postoperative Anesthesia Vital signs

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-02-14

Study Completion:2026-01-06

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT06133140

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Are expected to be admitted to one of the wards equipped with the GE Portrait Mobile Monitoring Solution; 2. Are ≥18 years old; 3. Are designated American Society of Anesthesiologists physical status 1-4; 4. Are scheduled for major noncardiac surgery lasting at least 1.5 hours; 5. Are expected to remain hospitalized at least one postoperative night; 6. Are expected to have general or neuraxial anesthesia.	1. Have language, vision, or hearing impairments that might compromise continuous monitoring; 2. Are designated Do Not Resuscitate, hospice, or receiving end of life care; 3. Are expected to have telemetry monitoring; 4. Have previously participated in the study.

Inclusion Criteria

Exclusion Criteria

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

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

Contacts and Locations

Principal Investigator

Ryu Komatsu, MD

PRINCIPAL_INVESTIGATOR

The Cleveland Clinic

Study Locations (Sites)

Cleveland Clinic Foundation

Cleveland, Ohio, 44195

United States

Collaborators and Investigators

Sponsor: The Cleveland Clinic

Ryu Komatsu, MD, PRINCIPAL_INVESTIGATOR, The Cleveland Clinic

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-14

Study Completion Date2026-01-06

Study Record Updates

Study Start Date2024-02-14

Study Completion Date2026-01-06

Terms related to this study

Keywords Provided by Researchers

Postoperative
Anesthesia
Vital signs

Additional Relevant MeSH Terms

Postoperative Complications