Clin2
NCT05510830Possibly a fitNot yet recruiting

Biopsy-guided cervical procedure for persistent high-risk HPV

Human Papilloma Virus InfectionHuman Papilloma Virus IntegrationCervical Intraepithelial NeoplasiaCervical CancerCervical Conization

Part of Cancer, Infections, Women’s health & pregnancy clinical trials.

This study looks at doing a diagnostic cervical conization (a cone-shaped tissue biopsy) when HPV remains persistent and there are warning signs, but initial pathology does not show precancer. It aims to find hidden precancer earlier or better understand HPV-related changes that were missed.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
250 people
Ages
25 years to 70 years
Study type
Interventional

Who can take part

  • You were referred for colposcopy and cervical biopsy because your screening test was abnormal, and the biopsy showed no precancer lesions
  • Your clinician suspects precancer based on one or more risk signs (such as long-lasting HPV 16/18 infection, high HPV “integration” reading, or suspicious colposcopy findings)
  • Your HPV or test results must match specific higher-risk patterns (for example TCT results like ASC-H or HSIL, or certain cell changes)
  • You are not pregnant
  • You do not have suspected vaginal precancer, ongoing untreated cancers in other body systems, or active (acute) genital/anal infections

View the official record on ClinicalTrials.gov

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Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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