Clinical Trials Directory

Trials / Completed

CompletedNCT03638427

Screening for Cervical Intraepithelial Neoplasia Using Self-collected Menstrual Blood

Status
Completed
Phase
Study type
Observational
Enrollment
159 (actual)
Sponsor
Stanford University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate the feasibility and efficacy of assessing HR-HPV DNA and HPV E6/E7 mRNA via self-collected menstrual blood in a smart menstrual pad. In other words, can the investigators detect the high risk strains of the human papilloma virus (HPV) that are associated with cervical cancer in self-collected menstrual blood, as an alternative to collecting vaginal swabs.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTMenstrual Blood Analysis (Menstrual Blood Analysis)We will be testing women's menstrual blood to investigate the feasibility and efficacy of assessing HR-HPV DNA and HPV E6/E7 mRNA via self-collected menstrual blood from a menstrual pad.

Timeline

Start date
2019-01-01
Primary completion
2022-10-11
Completion
2022-11-30
First posted
2018-08-20
Last updated
2024-05-28
Results posted
2024-05-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03638427. Inclusion in this directory is not an endorsement.