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Search / Trial NCT02237326

Visual Inspection With Acetic Acid Compared to Lugol's Iodine in HIV-infected Women

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Sep 9, 2014

Trial Information

Current as of June 01, 2025

Completed

Keywords

Visual Inspection With Acetic Acid Visual Inspection With Lugol's Iodine Cervical Intraepithelial Neoplasia Cervical Cancer Screening Hiv Infected Women

ClinConnect Summary

Cervical cancer and HIV are intersecting epidemics that both disproportionately affect low-income women; the impact of the socioeconomic disparity and biologic synergy of these two diseases is seen dramatically in Kenya, where cervical cancer is the most common cancer killer. HIV-infected women are at increased risk for the development of cervical precancer and cancer, develop more aggressive lesions and are affected at younger ages. Although screening for and treatment of precancer has reduced the incidence of cervical cancer to close to zero in resource-rich countries, strategies are cost...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • 23-59
  • Intact cervix/uterus
  • no evidence of infection
  • ability to provide informed consent
  • Exclusion Criteria:
  • pregnant

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

Kisumu, Nyanza, Kenya

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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