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RECRUITING
NCT06367465

Feasibility and Acceptability of HCV Treatment in Pregnancy

Sponsor: Washington University School of Medicine

View on ClinicalTrials.gov

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

Interventions

DRUG

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