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Trials / Active Not Recruiting

Active Not RecruitingNCT04863703

Improvement of Portal Hypertension During Viral Suppression in Patients With Hepatitis Delta (IMPHROVE-D)

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
11 (estimated)
Sponsor
Hannover Medical School · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Portal hypertension (PH) is one of the key drivers of clinical deteoration in patients with liver cirrhosis. It has been demonstrated that antiviral therapy in patients with chronic hepatitis C infection leads to a decrease of PH and is associated with an improved outcome. Recently, Bulevirtide was approved for the treatment of patients coinfected with hepatitis B (HBV) and chronic hepatitis delta (HDV) infection, which helps to achieve viral supression in these patients. This study investigates the potential effects of viral supression on PH in patients with chronic HBV/HDV infection and liver cirrhosis.

Conditions

Interventions

TypeNameDescription
DRUGBulevirtidePatients with liver cirrhosis and HBV/HDV coinfection receive Bulevirtide as an antiviral therapy irrespective of the study, this study is observational.

Timeline

Start date
2021-05-07
Primary completion
2024-11-30
Completion
2026-12-31
First posted
2021-04-28
Last updated
2025-09-15

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04863703. Inclusion in this directory is not an endorsement.