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Study identifier: NCT06829602 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Syphilis  ·  Sponsor: McMaster University

PhaseNA
Planned participants77
Who can joinAll sexes, 13 Years to 49 Years
Healthy volunteersYes

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Njideka Sanya  ·  +1-905-521-2100  ·  sanyan@mcmaster.ca

Stacey Clark  ·  +1-905-521-2100  ·  clarksta@mcmaster.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Maternity Centre of HamiltonHamilton, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06829602