Treponemal Shedding, Load, and Viability, in Women and Men-who-have-sex-with-women-only With Early Infectious Syphilis: Implications for Transmission
NCT ID: NCT07300254
Last Updated: 2025-12-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
480 participants
OBSERVATIONAL
2025-12-01
2028-12-31
Brief Summary
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1. Patterns of Tp detection in women and men-who-have-sex-with-women only.
2. Whether detected Tp from each asymptomatic anatomical sites is viable
3. Duration of Tp detection and viability (alive and transmissible bacteria). Patients presenting to a participating sexual health service (overseas only) for management of suspected/confirmed early infectious syphilis will be eligible. During the routine clinical examination, participants will have additional oral and anal swabs, urine, vaginal swab (where relevant), penile skin swab (where relevant) and blood sample collected, in addition to the routine samples taken from the same sites and routine serology collected when syphilis is diagnosed.
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Cis-women with suspected or confirmed primary syphilis infection
Cis-women with suspected or confirmed primary syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Cis-women with suspected or confirmed secondary syphilis infection
Cis-women with suspected or confirmed secondary syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Cis-women with confirmed early-latent syphilis infection
Cis-women with confirmed early-latent syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Men-who-have-sex-with-women-only with suspected or confirmed primary syphilis infection
Men-who-have-sex-with-women-only with suspected or confirmed primary syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Men-who-have-sex-with-women-only with suspected or confirmed secondary syphilis infection
Men-who-have-sex-with-women-only with suspected or confirmed secondary syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Men-who-have-sex-with-women-only with confirmed early-latent syphilis infection
Men-who-have-sex-with-women-only with confirmed early-latent syphilis infection
No Intervention: Observational Cohort
No intervention: Observational study
Interventions
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No Intervention: Observational Cohort
No intervention: Observational study
Eligibility Criteria
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Inclusion Criteria
a. Untreated clinically suspected primary or secondary syphilis. i. Must have rash or lesion(s) clinically suggestive of early infectious syphilis infection.
ii. May have positive PCR result, positive Dark-ground Microscopy result, positive syphilis serology or positive point-of-care syphilis test, but these are not necessary at the time of enrolment.
b. Untreated early latent (no clinical signs indicative of primary or secondary syphilis) syphilis with positive syphilis serology or positive point-of-care test, and one or more of the following(11): i. A documented syphilis seroconversion within the prior 12 months. ii. A sustained (longer than 2 weeks) fourfold or greater increase in the titre in the prior 12 months in a person previously treated for syphilis.
iii. Unequivocal symptoms of primary or secondary syphilis within the prior 12 months.
iv. Contact in the prior 12 months with a sex partner who had untreated primary, secondary, or early latent syphilis.
v. Documented reactive nontreponemal and treponemal tests, and the only possible exposure occurred during the previous 12 months vi. RPR/VDRL titre \>= 1:64 5. Be willing and able to complete study procedures, including physical examination 6. Receiving syphilis treatment on the day of recruitment 7. Have sufficient language proficiency to understand the requirements of the study 8. Provide informed consent as per individual site's local ethics requirements
Exclusion Criteria
2. Individuals who have received antibiotic treatment within 1 month prior to enrolment, with the EXCEPTION of metronidazole.
3. Diagnosis of late latent syphilis (\>1 year) or latent syphilis of unknown duration.
18 Years
ALL
No
Sponsors
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Melbourne Sexual Health Centre
UNKNOWN
The Alfred
OTHER
Monash University
OTHER
Responsible Party
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Principal Investigators
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Janet Towns
Role: PRINCIPAL_INVESTIGATOR
Monash University
Locations
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Monash University
Melbourne, Victoria, Australia
Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality, China
Shanghai Skin Disease Hospital
Shanghai, Shanghai Municipality, China
Foundation for Professional Development
Pretoria, , South Africa
Burrell Street Clinic, Guy's and St Thomas'
London, , United Kingdom
Jefferiss Clinic St Mary's Hospital, Imperial College London
London, , United Kingdom
Mortimer Market Centre
London, , United Kingdom
London School of Hygiene & Tropical Medicine
London, , United Kingdom
Countries
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Central Contacts
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Other Identifiers
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MUCTC-24018
Identifier Type: -
Identifier Source: org_study_id