Clinical Research Directory
Browse clinical research sites, groups, and studies.
Feasibility and Acceptability of HCV Treatment in Pregnancy
Sponsor: Washington University School of Medicine
Summary
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.
Official title: Feasibility and Acceptability of Early Linkage to HCV Treatment in Pregnancy Feasibility and Acceptability of Early Linkage to HCV Treatment in Pregnancy
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2024-02-01
Completion Date
2026-02-28
Last Updated
2025-12-29
Healthy Volunteers
Not specified
Conditions
Interventions
Glecaprevir-pibrentasvir
Glecaprevir-pibrentasvir 100 mg / 40 mg 3 tab orally (PO) once daily for 56 days.
Locations (2)
Barnes Jewish Hospital
St Louis, Missouri, United States
Washington Univeristy
St Louis, Missouri, United States