Viewing Study NCT06169553



Ignite Creation Date: 2024-05-06 @ 7:52 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06169553
Status: NOT_YET_RECRUITING
Last Update Posted: 2023-12-13
First Post: 2023-11-23

Brief Title: The Injection-Related InfectionS IRIS Program
Sponsor: McMaster University
Organization: McMaster University

Study Overview

Official Title: The IRIS Program A Novel Pathway to Optimize Treatment of Injection-related Infections for People Who Inject Drugs in Hamilton Ontario
Status: NOT_YET_RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: IRIS
Brief Summary: People who inject drugs are at risk of injection-related infections like abscesses or infective endocarditis The Injection-Related InfectionS IRIS program hopes to improve treatment for participants by providing a low-barrier one-stop shop model for people who inject drugs who experience injection-related infections to access more holistic and compassionate care IRIS is a non-randomized clinical trial meaning that it offers a specific program to eligible patients This program offers care for substance use and infectious disease with additional peer support and systems navigation if interested The investigators anticipate enrolling 80 participants in the intervention and will follow participants throughout the infection treatment period estimated 6-12 weeks The investigators will collect information at the time of enrolment at the 6-month mark and monthly via electronic medical chart review The investigators will use an interrupted time series analysis to evaluate the impact of the intervention on rates of treatment completion emergency department visits hospitalizations and death before versus after the intervention
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None