CompletedNot applicableNCT07498153
Spotting Syphilis: A Dual Point-of-Care Syphilis Screening Initiative in a Low-Resource Healthcare Setting
Studying Congenital syphilis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The University of Texas Health Science Center, Houston
- Principal Investigator
- Irene A Stafford, M.D., M.S., M.P.HThe University of Texas Health Science Center, Houston
- Intervention
- Chembio HIV/Syphilis rapid POC test(device)
- Enrollment
- 149 enrolled
- Eligibility
- 14-65 years · FEMALE
- Timeline
- 2025 – 2025
Study locations (1)
- The University of Texas Health Science Center at Houston, Houston, Texas, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT07498153 on ClinicalTrials.govOther trials for Congenital syphilis
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