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Transitional Care Study 3 — TRICA  

Surgery--Complications Clinical Trial

Official title:
PJ-013483 FLAGSHIP Transitional Care Study 3

Clinical Trial Summary

In this study patients with elective surgery will wear two devices (HealthDot and Elan) after surgery in hospital and after discharge at home for up to 2 weeks (HealthDot) or 3 weeks (Elan). The HealthDot will measure heart rate, posture, activity and respiratory rate which are stored on the device as well as sent to Philips. The Elan device will measure PPG and accelerometer data which is transferred to Philips. The data collected will be used for algorithm development. Data will be analysed retrospectively and compared to readmission and adverse events to see if the events could have been predicted due to the collected data by the devices. No clinical decisions will be based on the measurements done during the study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03923127
Study type Interventional
Source Philips Electronics Nederland B.V. acting through Philips CTO organization
Contact
Status Completed
Phase N/A
Start date April 16, 2019
Completion date August 17, 2020
View Details
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