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Clinical Trial Summary

The purpose of this study is to determinate the AMH levels before and after antiviral therapy with Ombitasvir-Paritaprevir-Ritonavir and Dasabuvir in comparison with age-matched HCV-positive women not undergoing antiviral treatment.


Clinical Trial Description

The study is interventional, controlled randomized (block 2:1 case: controls) in open label. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02950870
Study type Interventional
Source University of Modena and Reggio Emilia
Contact ERICA VILLA, Prof.
Phone +39 0594224359
Email erica.villa@unimore.it
Status Not yet recruiting
Phase Phase 4
Start date December 2016
Completion date December 2019