Improving Perinatal Outcomes Among Kenyan Pregnant Women With an Integrated STI Testing Model

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 universally vs. only among women without STI symptoms. All women with STIs detected and/or symptoms per Ministry of Health algorithms will receive immediate treatment, EPT per national guidelines, and tests of cure. All participants will be enrolled during routine antenatal care and followed through 9-months postpartum. The investigators will quantify and compare a composite outcome of pregnancy loss/stillbirth, PTB, LBW, SGA, and neonatal death, between randomization arms, in addition to several secondary and exploratory outcomes.

Eligibility
Participation Requirements
Sex: Female
Healthy Volunteers: t
View:

• 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 informed consent for participation

Locations
Other Locations
Kenya
Homa Bay Teaching and Referral Hospital
RECRUITING
Homa Bay
Rachuonyo South Sub County Hospital
RECRUITING
Homa Bay
Rangwe Sub County Hospital
RECRUITING
Homa Bay
Chulaimbo County hospital
RECRUITING
Kisumu
Kisumu County Hospital
RECRUITING
Kisumu
Lumumba Sub County hospital
RECRUITING
Kisumu
Migosi Sub County Hospital
RECRUITING
Kisumu
Yala sub County Hospital
RECRUITING
Yala
Contact Information
Primary
Lauren Gomez
gomezL4@uw.edu
206-685-5044
Backup
Felix Abuna
fabuna@uw.edu
+254 721 230652
Time Frame
Start Date: 2025-01-27
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 3132
Treatments
No_intervention: Standard of Care
In all arms, participants will receive syndromic STI assessment from study nurses at the antenatal clinic per Kenyan national guidelines, which entails a clinician (i.e., nurse, physician, clinical officer) using an algorithm asking whether clients have symptoms of vaginal discharge, lower abdominal pain, or genital ulcers followed by a physical examination for signs that match the self-reported symptoms. Based on clinical presentation, treatment is prescribed. Study nurses will capture information on symptoms, treatment acceptance, and dispensation. All participants will be provided with a study phone number to call at any time free of charge for clarifying questions or concerns with STI medication use.
Experimental: Universal Testing
Participants randomized to universal STI testing will be offered Xpert® CT/NG and TV testing regardless of symptoms, and they will receive a standard syndromic STI assessment.
Experimental: Asymptomatic Only Testing
Participants randomized to the asymptomatic only testing will be offered Xpert® CT/NG and TV testing if no signs or symptoms of CT, NG, or TV are identified during STI assessment.
Related Therapeutic Areas
Sponsors
Leads: University of Washington
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

This content was sourced from clinicaltrials.gov