Biomarkers and clinical scores in critically ill patients at the emergency department

Not Applicable

Recruiting

• Conditions: Delirium; F05.9

• Registration Number: RBR-233bct
• Lead Sponsor: Fundação de Amparo a Pesquisa do Estado de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-02-10
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Volunteers; Admitted to the Emergency Department for any acute illness; Patients hospitalized for less than 24 hours; Patients over 65 years

Exclusion Criteria

Hospitalization for exclusive palliative care or end-of-life care; Expected hospital stay less than 48 hours; Hospitalization for less than 30 days; Refusal of the patient or his representative to sign an informed consent form.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to correlate serum levels of brain injury biomarkers with Delirium diagnosis in patients admitted to the Emergency Department.

Secondary Outcome Measures

Name	Time	Method
It is expected to correlate serum levels of brain injury biomarkers with the prognosis of patients admitted to the Emergency Department;It is expected to correlate the intestinal microbiota profile with the diagnosis of delirium in patients admitted to the Emergency Department.