RecruitingNCT05368974

The Treatment in Pregnancy for Hepatitis C ("TiP-HepC") Registry

An Observational Study of Mother-Infant Outcomes Following Antenatal Exposure to Direct-Acting Antivirals: the Treatment in Pregnancy for Hepatitis C ("TiP-HepC") Registry


Sponsor

The Task Force for Global Health

Enrollment

100 participants

Start Date

Feb 11, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

Clinical interventions to reduce the risk of vertical transmission of hepatitis C virus (HCV) infection from mother to infant are highly limited. Direct-acting antiviral (DAA) medications have demonstrated excellent safety and efficacy in non-pregnant individuals, but there is a lack of data regarding the safety of these medications in pregnant women and the effectiveness of these medications in reducing mother-to-child transmission. Therefore, although HCV screening during pregnancy is now recommended in many countries, there is no approved treatment for HCV during pregnancy. An observational study is here proposed to assess outcomes of mother-infant pairs exposed to DAAs during pregnancy within a global clinical case registry. Data regarding the exposures and outcomes of mother-infant pairs exposed to DAAs during pregnancy will be solicited and collected from clinical providers, healthcare facilities, HCV treatment programs, and other clinical practices worldwide. Data will be shared and maintained within a secure database, and cumulative data will be analyzed at pre-determined six-month intervals. The primary outcome will be the number and proportion of mother-infant pairs with adverse pregnancy or birth outcomes. The results of this study will inform HCV treatment decisions by clinical providers and programs worldwide.


Eligibility

Plain Language Summary

Simplified for easier understanding

This is a registry study collecting information about pregnant women who were treated for hepatitis C (a liver infection caused by a virus) with direct-acting antiviral (DAA) drugs. The goal is to track pregnancy and baby outcomes in women who were accidentally or knowingly exposed to these medications during pregnancy. **You may be eligible if...** - You were pregnant and have a confirmed hepatitis C infection (diagnosed by RNA or core antigen testing) - You were exposed to a direct-acting antiviral (DAA) hepatitis C medication within 30 days of conception and before the end of the pregnancy **You may NOT be eligible if...** - Your hepatitis C treatment included ribavirin or interferon, which are known to be harmful during pregnancy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDirect Acting Antivirals

Direct-acting antiviral exposure during documented pregnancy


Locations(1)

The Taskforce for Global Health

Atlanta, Georgia, United States

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NCT05368974


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