RWE Study in the Treatment of Cervical Lesions of Various Etiology

Status Completed

Clinical Trial Summary

The aim of the study was to assess the post-market performance and tolerability of Cerviron® ovules in the treatment and management of cervical lesions of different etiologies. The study included clinical data related to aspect of lesions performed during routine colposcopy exams, the degree of re-epithelialization of the cervical mucosa, vaginal pH, pain level, and vaginal bleeding level.

Clinical Trial Description

This study is an observational, post-marketing study conducted between May-July 2021. The aim of the study was to assess the post-market performance and tolerability of Cerviron® ovules in the treatment and management of cervical lesions of different etiologies. The secondary objective of this clinical investigation is the assessment of performance of the medical device by clinical exam and patients' degree of satisfaction related to the use of the medical device. The study population included 345 participants aged 20-70 years with either a cervical lesion under treatment or with recent surgical removal of a cervical lesion. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05668806
Study type	Observational
Source	Perfect Care Distribution
Contact
Status	Completed
Phase
Start date	May 20, 2021
Completion date	July 31, 2021

View Details

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