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NCT05593692 Clinical Trial

Gender Differences and Age Related Differences in Emergency Department Admission

Emergencies Clinical Trial

— SADE  

Official title:
Gender Differences and Age Related Differences in Emergency Department Admission

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05593692
Other study ID # 5121
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 18, 2022
Est. completion date December 28, 2024

Study information
Verified date February 2024
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Marcello Covino
Phone 00390630153188
Email marcello.covino@policlinicogemelli.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about difference related to age and gender in patients admitted to emergency department.

Description:

Objectives: Medicine is progressively becoming aware of the clinical difference among patients who present different age, gender, and comorbidities. Our goal is to examine how often different groups of patients access the Emergency Department and for which causes, as well as their different hospitalization and death rates. Materials and methods: The investigators will collect and analyze data from all patients evaluated at the emergency department of "Fondazione Policlinico Agostino Gemelli" and "Istituto Clinico Humanitas di Milano" from January 2014 to December 2023, the sample obtained will be divided into four groups: younger than 50 years old, 50-65 years old, 66.75 years old, older than 75; each of these groups is divided between males, females and people who do not identify with either of those genders

Recruitment information / eligibility
Status Recruiting
Enrollment 15000
Est. completion date December 28, 2024
Est. primary completion date September 5, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age over 18 y - Admitted to emergency department Exclusion Criteria: - Age under 18 y

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Italy IRCSS Fondazione Policlinico Agostino Gemelli Roma Lazio

Sponsors (1)
Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Primary Death Death 30 days
Secondary length of stay length of stay 180 days
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