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Study identifier: NCT07729891 Synced from ClinicalTrials.gov · July 29, 2026
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Real-time Evaluation and Continuous Observation of Vital Signs for Enhanced Recovery: a Study for the Early Identification of Complications in the Surgical Ward Following Surgery in Patients Not Eligible for Intensive Care Admission.

Condition: Postoperative Complication · Respiratory Complications · Cardiac Complications  ·  Sponsor: Azienda Ospedaliero-Universitaria di Parma

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to evaluate whether continuous vital sign monitoring with wearable devices can help detect postoperative complications in surgical ward earlier than standard hospital monitoring. In particular, the goal of this observational study is to evaluate if the wireless wearable devices Portrait Mobile (GE Healthcare) can detect early signs of complications after major urologic surgery in adults who are not eligible for intensive care unit admission. The main questions it aims to answer are: * Can continuous monitoring of vital signs (heart rate, breathing rate, blood oxygen) detect health problems earlier than standard nurse checks in the urology ward? * How many times do participants' vital signs change in ways that suggest a complication is developing during the first days after surgery? * Does the vital sign trend and/or the deviation from patients' baseline suggest a complication is developing during the first days after surgery? * Does continuous monitoring help healthcare providers intervene before patients become critically ill thus reducing complications burden or severity and reducing unplanned intensive care admission? Participants in the intervention cohort will wear a wireless patch-like device on their chest that continuously tracks their heart rate, breathing rate, and blood oxygen levels. The device sends this information to hospital staff through a secure wireless connection while participants recover in the regular urology ward after surgery. Partici…

This description comes directly from the study's public registry record.

Talk to the study team

Valentina Bellini  ·  +393388284629  ·  bellini.vnt@gmail.com

Matteo Panizzi  ·  +393494156020  ·  matteo.panizzi@unipr.it

Always discuss trial participation with your own doctor first.

Locations (1)

2^ Anestesia, Rianimazione, Terapia Intensiva - Azienda Ospedaliero Universitaria di ParmaParma, Parma, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT07729891