Human Papilloma Virus-Related Cervical Carcinoma

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Review clinical trials related to Human Papilloma Virus-Related Cervical Carcinoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The Women's Screening and Self-Testing Program (PROMETA) Study

This proposal directly addresses the ability to safely scale-up a Screen-Triage-Treat approach to cervical cancer screening. The investigators propose to capitalize on a pool of screen-eligible women accessing routine care within targeted human immunodeficiency virus (HIV) care and treatment services. The primary outcome of interest is the number of women screened and the proportion of screen-positive women undergoing treatment. Secondary outcomes will focus on other implementation outcomes, and if successful, will be utilized to inform future research to take this approach to scale across Mozambique.

Participants needed: 8,445
Trial details
Age: 25-49Biological sex: FemaleType: InterventionalSponsor: Tulane UniversityUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

Women 25-49 years [+3]

Physical or mental impairment that inhibits participation in the study [+2]