About this trial
The goal of this observational study is to learn about the effectiveness of the multi-modal evaluation for agitation behavior in critically ill patients based on remote video-Ultra-sensitive detection wave.
The main question it aims to answer is: evaluate the effectiveness of multi-modal evaluation monitoring system for agitated critically ill patients Participants already taking multi-modal evaluation monitoring system as part of their regular medical care for agitated critically ill patients will compare their effectiveness for agitation for 3 years.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients at risk of agitation in the ICU
Patients with RASS score -2 and above
≦ 65 years old, ≧ 18 years old
Disqualifiers
The affected party refused to participate in this study
Missing/incomplete information
Vulnerable groups such as pregnant women, those who lack the capacity for civil conduct and do not have the consent of their legal representatives
Maxillofacial trauma, burns, tumors, surgery, etc. affect facial expression
Trial population
any patients with agitation
Trial design
Case-control
Prospective
Treatments tested in this trial
multi-model monitoring and alert
Diagnostic testAll agitated critically illed patients are monitored by manual and multi-model monitoring and alert system
Treatment groups
Trial outcomes
Primary outcomes
the correct rate for alerting agitated critically ill patients
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead sponsor
People's Hospital of Quzhou
Collaborator
The Second Affiliated Hospital of Jiaxing University
Collaborator
Zhoushan Hospital of Zhejiang
Collaborator
Longquan People's Hospital
Collaborator
Fuyang District First People's Hospital of Hangzhou
Collaborator
The Third Affiliated Hospital of Wenzhou Medical University
Collaborator