Offering Routine and Rapid Point of Care (POC) Syphilis Testing in Pregnant Patients Presenting to the Emergency Department

Recruiting N/A Interventional Study
Syphilis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 50
Sex
Female
Study type
Interventional
Purpose
Diagnostic
Participants needed
1,500 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial
The purpose of this study is to offer routine lab-based and rapid point of care (POC) syphilis diagnostic testing in the emergency department (ED) and obstetrical (OB) triage , thereby increasing screening and treatment initiation for pregnant patients without prenatal care or with no documented syphilis results during the index pregnancy in other to increase rates of full treatment to determine i…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Pregnant individuals that are seeking care at University of Texas, Memorial Herman and Lyndon B Johnson sites ED or obstetrical triage units. * No Prenatal care during index pregnancy * No documented syphilis result during the index pregnancy Exclusion Criteria: * Pregnant i…
Contacts

Irene Stafford, MD

(713) 500-6412

Irene.Stafford@uth.tmc.edu

CONTACT

Carrie Bakunas, MD

(713) 500-7878

Carrie.A.Bakunas@uth.tmc.edu

CONTACT