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NOT YET RECRUITING
NCT07733557
NA

HPV Detection Using Self-Collected Menstrual Blood

Sponsor: Samantha Batman

View on ClinicalTrials.gov

Summary

This study is evaluating whether human papillomavirus (HPV) can be accurately detected from self-collected menstrual blood samples. Participants who have had routine clinical HPV testing within the previous 90 days will collect a menstrual blood sample at home using a study-provided collection kit. The HPV test result from the menstrual blood sample will be compared with the participant's prior clinical HPV test result to assess agreement between the two methods. The goal is to determine whether menstrual blood collection may provide a feasible, noninvasive approach for HPV testing.

Official title: Concordance of HPV Detection Using Self-Collected Menstrual Blood

Key Details

Gender

FEMALE

Age Range

21 Years - 49 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2026-07

Completion Date

2029-07

Last Updated

2026-07-29

Healthy Volunteers

No

Interventions

DEVICE

Endometrics Menstrual Blood Collection Kit

Investigational self-collection menstrual blood sampling kit used to collect menstrual blood specimens for HPV testing and concordance assessment with prior routine clinical HPV test results.

Locations (1)

University of Virginia

Charlottesville, Virginia, United States