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Postoperative Complications in Cancer Patients Monitored With Intelligent Continuous Monitoring System
Sponsor: Rigshospitalet, Denmark
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
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