Does Continuous Vital Sign Monitoring Increase Investigations and Interventions in Complication-free Patients?

NCT06361862 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 700

Last updated 2025-04-06

No results posted yet for this study

Summary

This aim of this study is to investigate whether active alerts during CVSM result in an increased number of diagnostic tests and treatments in complication free patients, hypothesizing that more interventions are performed in the CVSM-group than standard of care (EWS) group.

Conditions

Interventions

DEVICE

Active alarms from WARD software

Wireless continuous vital sign monitoring with real time staff alerts

Sponsors & Collaborators

  • Bispebjerg Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2025-04-02
Completion
2025-04-02

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06361862 on ClinicalTrials.gov