the Multi-modal Evaluation of Agitation in Critically Ill Patients Based on Remote Video-Ultra-sensitive Detection Wave

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

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 volunteers

Qualifiers

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

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • multi-model monitoring and alert

    Diagnostic test

    All agitated critically illed patients are monitored by manual and multi-model monitoring and alert system

Treatment groups

580 Participants
are divided into 2 treatment groups
Group A: control group: monitoring by manual way0 interventions
Group B: multiple-model monitoring group: agitation monitoring by remote video-radar wave1 intervention

Trial outcomes

Primary outcomes

1

the correct rate for alerting agitated critically ill patients

Time frame
10-15 seconds every agitated patients during stay in ICU

Secondary outcomes

Other outcomes

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