Global Burden Estimation of Human Papillomavirus (GLOBE-HPV)
Launched by INTERNATIONAL VACCINE INSTITUTE · Nov 10, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The GLOBE-HPV trial is an important study looking at how common high-risk types of Human Papillomavirus (HPV) are among girls and women aged 9 to 50 years in various countries, including some in South Asia and sub-Saharan Africa. The study aims to gather information through surveys to understand how many women have HPV and how often it lasts, especially in young women who are sexually active. It will also include smaller studies to explore factors like gender roles and social stigma that may affect women’s access to HPV prevention, screening, and treatment services.
To participate in this study, women need to be between 9 and 50 years old and have lived in the selected community for at least three months. Those who are 18 or older can provide their own consent, while younger participants will need permission from a parent or guardian. If you join the study, you can expect to answer some questions and possibly provide samples for testing. Overall, this trial aims to gather crucial data that can help improve HPV prevention and care for women in the participating regions.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • 1. 9 to 50 years old (for urban and rural CSSs) at the time of enrollment.
- • 2. Resident in the selected community for at least the past 3 months (with the exception of pastoralists, refugees, and commercial sex workers).
- • 3. Able to understand the purpose of the study and study procedures.
- • 4. If aged 18 years or older or legally considered an emancipated minor, able and willing to provide consent to participate in the study including sample collection.
- • 5. If aged \<18 years (and not considered an emancipated minor), supported in their participation by a parent or guardian who is able and willing to provide consent, and
- • 6. If aged \<18 years (and not considered an emancipated minor), able and willing to provide assent to participate in the study.
- Exclusion Criteria:
- • 1. Decline consent to participate any activity of the study.
- • 2. A medical condition or other reason, not directly related to HPV infection or HPV-related diseases, in the opinion of the investigator, precludes enrolment in the study.
About International Vaccine Institute
The International Vaccine Institute (IVI) is a non-profit organization dedicated to advancing global health through the development and delivery of innovative vaccines. Established in 1997 and headquartered in Seoul, South Korea, IVI collaborates with governments, academic institutions, and industry partners to conduct research and clinical trials aimed at preventing infectious diseases prevalent in low- and middle-income countries. By leveraging its expertise in vaccine development, IVI strives to enhance vaccine accessibility and affordability, ultimately contributing to the reduction of morbidity and mortality associated with vaccine-preventable diseases worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lusaka, , Zambia
Dhaka, , Bangladesh
Kinshasa, , Congo, The Democratic Republic Of The
Ho, Volta, Ghana
Dhulikhel, , Nepal
Karachi, , Pakistan
Freetown, , Sierra Leone
Mwanza, , Tanzania
Patients applied
Trial Officials
Alexandra Hill
Principal Investigator
Associate Research Scientist
Deborah Watson-Jones
Principal Investigator
Professor of Clinical Epidemiology & International Health
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported