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RECRUITING
NCT06829602
NA

The Feasibility of Implementing Syphilis Point-of-care Testing Into a Prenatal Clinic for People Facing Barriers to Care

Sponsor: McMaster University

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn if a finger-prick blood test for rapid diagnosis of syphilis infection can be implemented in a low-barrier prenatal clinic for people at risk of syphilis in pregnancy. The test gives results in 5 minutes and also tests for HIV. The main questions the study aims to answer are: * How often do pregnant people at risk of syphilis agree to the rapid test? * How well do healthcare providers perform the rapid test? * Does the rapid test speed up diagnosis and treatment of syphilis in pregnant people and their sexual partners? Participants will: * Give feedback about why they did or did not want to take the rapid test, and what their experience was taking the test; and * Share information about their health, pregnancy, and syphilis treatment (if applicable).

Official title: PREnatal Syphilis Point-of-care ScreenING in an Urban Low-barrier Clinic: A Prospective Single Arm Feasibility Trial

Key Details

Gender

All

Age Range

13 Years - 49 Years

Study Type

INTERVENTIONAL

Enrollment

77

Start Date

2025-06-25

Completion Date

2026-05

Last Updated

2025-07-06

Healthy Volunteers

Yes

Conditions

Interventions

DIAGNOSTIC_TEST

Rapid Syphilis/HIV point-of-care test

The INSTI Multiplex HIV/Syphilis Duo Antibody Test is a rapid immunoassay that can detect HIV and syphilis antibodies in the blood using finger-prick blood samples. The test is Health Canada-approved.

Locations (1)

Maternity Centre of Hamilton

Hamilton, Ontario, Canada