Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Feasibility and Acceptability of HCV Treatment in Pregnancy

Key facts

Where
St Louis, United StatesSee the 2 sites

Where in United States

  • Barnes-Jewish HospitalSt Louis, United StatesContact: Tracey BachTaking people
  • Washington UniveristySt Louis, United StatesContact: Laura Marks, MD,PhDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Washington University School of Medicine
Trial code
NCT06367465
Record updated
9 June 2026
Original description
Pregnant adults over the age of 18 who are seen in the Washington University obstetrics and gynecology, maternal fetal medicine or infectious diseases clinic or admitted to BJH with hepatitis C virus infection who have a history of past or current drug useRead full original descriptionShow less

Feasibility and Acceptability of Early Linkage to HCV Treatment in Pregnancy Feasibility and Acceptability of Early Linkage to HCV Treatment in Pregnancy

Pregnant adults over the age of 18 who are seen in the Washington University obstetrics and gynecology, maternal fetal medicine or infectious diseases clinic or admitted to BJH with hepatitis C virus infection who have a history of past or current drug use

Participant Duration: Approximately 1 year.

Aims:

Aim 1 - Evaluate adherence and treatment completion rates when glecaprevir-pibrentasvir is started during pregnancy for women who use drugs.

Aim 2 - Evaluate patient experience with hepatitis C virus treatment during pregnancy.

Inclusion: 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: -.

ClinicalTrials.gov NCT06367465