Personalised Real-time Interoperable Sepsis Monitoring (PRISM)
NCT: NCT06238180 · WITHDRAWN
Brief Summary
The goal of this prospective observational study is to develop and utilize an Artificial Intelligence (AI) model for the prediction of postoperative sepsis in patients undergoing abdominal surgery. The main questions it aims to answer are: 1. Can a remote AI-driven monitoring system accurately predict sepsis risk in postoperative patients? 2. How effectively can this system integrate and analyze multimodal data for early sepsis detection in the surgical ward? Participants are equipped with non-invasive PPG-based wearable devices to continuously monitor vital signs and collect high-quality clinical data. This data, along with demographic and laboratory information from the Electronic Health Record (EHR) of the hospital, are used for AI model development and validation.
Frequently Asked Questions
What is Personalised Real-time Interoperable Sepsis Monitoring (PRISM)?
Personalised Real-time Interoperable Sepsis Monitoring (PRISM) is a clinical trial registered under NCT06238180. Current status: WITHDRAWN.
What is the status of NCT06238180?
The current status of NCT06238180 (Personalised Real-time Interoperable Sepsis Monitoring (PRISM)) is: WITHDRAWN.
When did Personalised Real-time Interoperable Sepsis Monitoring (PRISM) start?
Personalised Real-time Interoperable Sepsis Monitoring (PRISM) started on 2023-11-29.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.