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Trials / Recruiting

RecruitingNCT06147388

Regression of Cervical Precancerous Lesions and Associated Risk Factors

Status
Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
General University Hospital, Prague · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers

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.

Detailed description

Introduction There are three grades of dysplasia of the cervix based on their severity (CIN 1-3). Most women with CIN 2 or CIN 3 (high-grade - HG lesions) are referred for conization due to the presumed risk of developing invasive cervical cancer. However, this surgical intervention is associated with an increased risk of preterm labor in the future. From the literature, it is evident that 30% - 60% of CIN 2 and CIN 3 lesions spontaneously regress. Colposcopic examination is a tool that can accurately assess the severity of the lesion and safely evaluate the dynamics of its development. It can be used to exclude the presence of invasive cervical cancer. The aim of the study is to determine the absolute rate of spontaneous regression of HG lesions, considering stratification factors. Methods Patients meeting all inclusion criteria and none of the exclusion criteria are included (see below). Colposcopic evaluations occur at four-month intervals during the study. In case of progression, the patient is indicated for conization; in case of persistence, the patient is consulted and can choose further observation or conization; in case of regression, punch biopsy is performed to acquire a histopathologic sample for primary endpoint evaluation. The biopsy/conization result is subsequently compared with the initial sample to declare regression or persistence of the HG lesion. The HPV status and cytological findings are evaluated similarly. Stratification criteria such as age, colposcopic characteristics, HPV genotype (Cobas 4800, Roche Molecular Systems, Pleasanton, USA), methylation markers (GynTect®, Oncgnostics GmbH, Löbstedter Str. 41, 07749 Jena, Germany), semiquantitative microscopic assessment of the vaginal swab, and personal history are assessed during monitoring.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTColposcopyNo surgery, observation

Timeline

Start date
2022-09-01
Primary completion
2026-07-01
Completion
2027-07-01
First posted
2023-11-27
Last updated
2026-02-25

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT06147388. Inclusion in this directory is not an endorsement.