Condition: HPV Infection · HPV 16 Infection · High Risk HPV · Sponsor: Qurasense
The EQUIP Study is testing whether high-risk human papillomavirus (hrHPV), the virus that causes most cervical cancers, can be accurately detected from menstrual blood collected at home. People who have been referred for colposcopy after an abnormal Pap or hrHPV test will use the Q-Pad Kit during their period to collect menstrual samples on a special menstrual pad and mail them to a central laboratory for hrHPV testing. The same participants will have a standard cervical sample collected for routine hrHPV testing and will undergo colposcopy as part of their usual care. By comparing hrHPV results from menstrual samples with results from cervical samples and biopsy findings, the study will evaluate how well the Q-Pad hrHPV Test System detects cervical precancer and will also assess how easy and acceptable it is for participants to use this at-home collection method.
This description comes directly from the study's public registry record.
Brian Weinberg, MS · 833-367-7846 · care@qvin.com
Always discuss trial participation with your own doctor first.
| Planned Parenthood of Southern New England | New Haven, Connecticut, United States | Recruiting |
| Planned Parenthood North Central States | Minneapolis, Minnesota, United States | Recruiting |
| Planned Parenthood of Greater Ohio (PPGOH) | Akron, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07281599