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Clinical Trials/IRCT2017071128308N3
IRCT2017071128308N3CompletedPhase 2

The effect of adding Irbesartan to Pegylated Interferon-alpha-2a in Patients With HBeAg Negative Chronic Hepatitis B Co-infected With Hepatitis D

Vice chancellor for research Tehran University of Medical Sciences0 sites45 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
45

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 69 years (—)
Sex
All

Inclusion Criteria

  • chronic hepatitis B with HBsAg present at least 6 months before screening and infection with hepatitis D virus as anti-HDV positive antibodies for at least 3 months and positive for HDV-RNA in the screening period; HBeAg negative ; All women with fertility potential should have a negative pregnancy test before enrollment; ability to provide informed written consent to participate in the study.Exclusion criteria: untreated liver disease; co-infection with hepatitis C or HIV; Creatinine clearance <60 ml / min; Patients who are allergic to one of the Irbesartan components; Pregnancy and lactation; Patients with SBP <110 mm Hg or history of hypo tension at any time

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice chancellor for research Tehran University of Medical Sciences

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