Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06269198
NA

Postoperative Complications in Cancer Patients Monitored With Intelligent Continuous Monitoring System

Sponsor: Rigshospitalet, Denmark

View on ClinicalTrials.gov

Summary

The primary objective of this study is to determine the effect on complication severity of using a clinical monitoring system with automatic vital sign alerts in addition to routine monitoring versus routine monitoring alone in high-risk postoperative cancer patients within 30 days after surgery. Other objectives include documentation of the severity of complications within seven days of surgery, frequency of serious adverse events, mortality, length of stay and delay of planned chemotherapy.

Official title: Postoperative Complications in Cancer Patients Monitored With Intelligent Continuous Monitoring System Versus Standard of Care - a Randomized Clinical Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

504

Start Date

2023-10-31

Completion Date

2027-04-01

Last Updated

2025-01-15

Healthy Volunteers

No

Interventions

DEVICE

WARD-CSS

Patients' continuously monitored vital signs will be recorded via a bedside tablet device (data not visible). The clinical staff will have access to the continuously monitored vital signs through a mobile device (smart phone) with a purpose-built app-based GUI displaying vital sign status and summaries, alarms, and device connectivity. The GUI will alert the clinical staff (acoustic and visual signals) when any of the predefined thresholds for deviating vital signs are exceeded.

Locations (3)

Copenhagen University hospital - Rigshospitalet

Copenhagen, Other (Non US), Denmark

Bispebjerg Hospital

Copenhagen, Other (Non US), Denmark

Hvidovre Hospital

Hvidovre, Other (Non US), Denmark