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OpenTrials
Completed

NCT Number: NCT01506128

Human Papillomavirus in Menstrual Blood

The investigators tried to know whether a virus causing cervical cancer could be detected in menstrual blood and to set up a experimental setting to detect the virus.

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Key information

Conditions

Human Papillomavirus

Sex eligibility

Female

Study type

Observational

Primary location

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Premenopausal women with HSIL at Pap test or high-risk HPV

Exclusion criteria

  • Suspicious cancer

Treatment and study plan

Collecting a Pad used at the first menstrual period after enrollment

Other

Collecting a Pad used at the first menstrual period after enrollment

Primary outcomes

  1. HPV detection rate in menstrual blood

    Time frame: First period after enrollment usually within 2 months after enrollment

    The first menstrual period after enrollment is assumed to occur within 2 months. At that time, the participant used pads and send the used pads to investigators. The investigator do procedures to detect HPV in pads.

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Official study title

Exploration of Optimal Experimental Settings to Detect Human Papillomavirus From Menstrual Blood in Women With High-grade Squamous Intraepithelial Lesion or High-risk Human Papillomavirus Infection

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jan 9, 2012
Registry last updated
Mar 5, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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