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Non-Invasive Plasma Treatment for Cervical Infections: Targeting High- and Low-Risk HPV Variants

Cervical Cancer Clinical Trial

Official title:
Treatment of Infections of the Cervix Uteri With High- and Low-risk Variants of the Human Papillomavirus Using Non-invasive Physical Plasma

Clinical Trial Summary

This is a prospective, single-center, observational proof-of-principle clinical trial at the Department of Women's Health of the University Hospital Tübingen.

Clinical Trial Description

The aim of this study is to investigate the HPV (Human papillomavirus)-eradicating efficacy of NIPP (non-invasive physical plasma) in patients with confirmed HPV infection but without cervical dysplasia. Another objective is to examine cellular/molecular/immunological effects of NIPP on the cervix through molecular biological methods following in-vivo treatment. Tissue samples will be obtained at defined intervals via minibiopsy, and analyses will be conducted using molecular biological, histological, and microscopic methods, potentially in collaboration with other research institutes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06291311
Study type Observational
Source University Hospital Tuebingen
Contact Martin Weiss, Dr. med.
Phone +497071 29 82211
Email martin.weiss@med.uni-tuebingen.de
Status Recruiting
Phase
Start date December 27, 2023
Completion date December 2025
View Details
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