A study of a wireless sensor (the Radius VSM biosensor) during surgery and recovery
Not Applicable
- Conditions
- Patients admitted at the surgical wardSurgery
- Registration Number
- ISRCTN56757048
- Lead Sponsor
- niversity Medical Center Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
1. Patients admitted to the surgical ward
2. Planned for surgery
3. 18 years or older
4. Expected hospital stay of at least 48 hours
Exclusion Criteria
1.Mentally incapable of participation
2.Unable to wear wearable devices
3.Postoperative ICU admission
4.No smartphone
5.Ambulatory or day surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reliability and accuracy <br>1. Presence (percent of time) of a continuous data-stream of vital parameters via the Masimo Radius VSM device: heart rate, blood pressure, oxygen saturation, respiration rate and skin temperature <br>2. Comparison of the numerical values of the Masimo Radius VSM versus vital parameter measurements from perioperative anesthetic monitoring and postoperative monitoring at the PACU <br>
- Secondary Outcome Measures
Name Time Method Clinical applicability <br>1.Data quality and data losses and how this is related to motion or physical activity <br>2.Vital parameters acquired during standard nursing rounds and MEWS data derived from rounds and computed by EMR <br>3.Patient reported pain scores and results from the daily QoR-15NL collected using RoQua (www.roqua.nl) and stored within the EMR <br>4.Incidence and moments of perioperative or postoperative complications <br>5.Incidence and moments of administration of (unexpected) drug therapy, e.g. i.v.-fluids, into tropics or antibiotics <br>6.Experiences of patients (satisfaction, barriers and potential benefits)<br>