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Recruiting NCT06147388

Regression of Cervical Precancerous Lesions and Associated Risk Factors

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Trial Parameters

Condition Cervix Uteri SIL
Sponsor General University Hospital, Prague
Study Type OBSERVATIONAL
Phase N/A
Enrollment 300
Sex FEMALE
Min Age 18 Years
Max Age 40 Years
Start Date 2022-09-01
Completion 2026-07-01
Interventions
Colposcopy

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Brief Summary

The aim of this study is to assess the extent of histopathological regression of severe cervical precancerous lesions (CIN 2 and CIN 3); evaluate the proportion of patients who experience the normalization of HPV test and cytology finding among those who were treated conservatively and those who underwent conization; and identify predictive parameters associated with regression. Based on this analysis, a model will be proposed to predict the likelihood of lesion regression.

Eligibility Criteria

Inclusion Criteria: 1. squamocolumnar junction fully visualized 2. bioptically verified CIN 2 or CIN 3 3. age ≥ 18 years 4. age ≤ 40 years 5. informed consent Exclusion Criteria: 1. squamocolumnar junction not fully visualized 2. suspicion on glandular lesion 3. suspicion on invasive cancer 4. personal history of CIN 2, 3 or cerv. cancer 5. gravidity 6. HIV positivity 7. immunosuppression 8. impossible photographic documentation

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