Improving Perinatal Outcomes Among Kenyan Pregnant Women With an Integrated STI Testing Model
Recruiting
N/A
Interventional Study
Hiv
Sexually Transmitted Infections (Not HIV or Hepatitis)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Sex
- Female
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 3,132 (estimated)
- Sponsor
- University of Washington · Other
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About This Trial
The investigators will conduct a 3-arm individual-level RCT in Kisumu and Siaya, Kenya to compare perinatal outcomes associated with 3 models of STI testing and management in antenatal care. The investigators will enroll 3132 pregnant women and randomize 1:1:1 to receive standard-of-care (syndromic management only without CT, NG, or TV testing) vs. CT, NG, and TV testing using Xpert® assays univer…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Self-identifying as a cisgender woman
* Seeking antenatal services from the clinic
* Planning to receive antenatal and postnatal care at the clinic
* Willingness to receive syndromic STI screening and HIV/syphilis testing per national guidelines
* Able and willing to provide i…
Contacts