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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03595527
Other study ID # 17.300
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2018
Est. completion date October 10, 2020

Study information

Verified date February 2023
Source Centre hospitalier de l'Université de Montréal (CHUM)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cross-sectional study of patients consulting in the emergency room of the Centre hospitalier de l'Université de Montréal (CHUM), to assess the implementation of an "opt-out" screening program for HIV and HCV and prospective follow-up for 3 months of positive cases.


Description:

The purpose of this study is to evaluate the feasibility of routine HIV and HCV screening using an "opt-out" approach at the emergency room of the CHUM and to determine the rate of new positive HIV and HCV cases. A sub-analysis will focus more specifically on HCV in the Quebec equivalent of "baby boomers" (1945-1975) since this is the group that was targeted in the United States. The second phase of this study will evaluate the effectiveness of the linkage to the healthcare system for people diagnosed with HIV or HCV and how fast these people are taken care of and put on treatment.


Recruitment information / eligibility

Status Completed
Enrollment 6350
Est. completion date October 10, 2020
Est. primary completion date October 10, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 73 Years
Eligibility Inclusion Criteria: - Individuals attending the emergency room of the Centre hospitalier de l'Université de Montréal Exclusion Criteria: - Individuals unable to opt-out due to their psychological or physical condition

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
HIV and HCV screening
HIV test: ARCHITECT HIV Ag/Ab Combo, Abbott HCV test: ARCHITECT Anti-HCV, Abbott

Locations

Country Name City State
Canada Centre Hospitalier de l'Université de Montréal Montréal Quebec

Sponsors (4)

Lead Sponsor Collaborator
Centre hospitalier de l'Université de Montréal (CHUM) Gilead Sciences, Merck Sharp & Dohme LLC, Ministere de la Sante et des Services Sociaux

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence Prevalence of HIV and HCV among patients who consult at the ER of the CHUM (overall and undiagnosed cases) 10 months
Secondary Prevalence Among Baby-boomers Determine the prevalence of new cases of HCV among "baby boomers" (1945 - 1975) 10 months
Secondary Opt-out Determine the percentage of patients that opted-out of the routine screening for HIV and HCV at the ER 10 months
Secondary Initial Workup Among patients with a newly positive HIV or HCV test in the ER, determine the percentage of those who attended a first workup appointment at 1 month 1 month
Secondary Cascade of Care Determine the percentage that completed certain steps of the HIV and HCV care cascades at 3 months, ie confirmation of diagnosis, liver fibrosis assessment (HCV), and treatment initiation (HIV) or prescription (HCV) 3 months
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