Evaluating hepatitis C treatment during pregnancy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on pregnant adults over 18 years old who have hepatitis C and a history of drug use. Participants will receive treatment with glecaprevir-pibrentasvir and will attend four in-person visits to assess treatment adherence and patient experience. The study aims to evaluate how well patients complete their treatment and their overall experience with the therapy during pregnancy. Standard care labs will be conducted throughout the study to monitor health outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Female patients ≥ 18 years old, pregnant at the time of study intake, diagnosed with hepatitis c virus infection and a history of past or current drug use.

Exclusion Criteria:

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Where it's running

• Barnes Jewish Hospital
  St Louis, Missouri, United States Recruiting
• Washington Univeristy
  St Louis, Missouri, United States Recruiting

Study contacts

• Study coordinator: Tracey Bach, MBA
• Email: habrockt@wustl.edu
• Phone: 314-273-6075

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.