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The Injection-Related InfectionS (IRIS) Program

McMaster University logo

McMaster University

Status

Not yet enrolling

Conditions

Injection-related Infections
Peer Support
People Who Infect Drugs (PWID)
Infections

Treatments

Other: Holistic injection-related injection treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT06169553
HAH-23-012

Details and patient eligibility

About

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.

Enrollment

80 estimated patients

Sex

All

Ages

16 to 105 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 16 or older
  • Able to provide informed consent
  • Presenting with a confirmed or suspected injection-related infection (including skin and soft tissue infections, osteomyelitis, infective endocarditis, Hepatitis C, HIV, etc)
  • History of injection drug use within 3 months of recruitment
  • Lives in Hamilton, Ontario

Exclusion criteria

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

Intervention group
Experimental group
Description:
Participants in the IRIS program will be offered a one-stop, low-barrier combined care model to address their injection-related infections. Specific program components include: (1) Diagnosis and treatment of injection-related infections; (2) Substance use treatment (3) Peer support; and (4) Care coordination/systems navigation.
Treatment:
Other: Holistic injection-related injection treatment

Trial contacts and locations

2

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Central trial contact

Alisha Atri

Data sourced from clinicaltrials.gov

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