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Clinical Trial Summary

Cervical intraepithelial neoplasia will be treated with physical low temperature plasma in the plasma cohort compared to watchful waiting in the control cohort. Primary endpoint after 3-6 months: Pathological remission. Secondary endpoint: HPV remission.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03218436
Study type Interventional
Source University Women's Hospital Tübingen
Contact
Status Active, not recruiting
Phase N/A
Start date August 31, 2017
Completion date July 1, 2021

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