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Therapeutic Efficacy of an Angiotensin II Receptor Antagonist in Patients with Nonalcoholic Steathepatitis

Therapeutic Efficacy of an Angiotensin II Receptor Antagonist in Patients with Nonalcoholic Steathepatitis - GLSG, 2004, ARB

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000202
Enrollment
10
Registered
2005-09-13
Start date
2004-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nonalcoholic steatohepatitis

Interventions

Angiotensin II receptor Antagonist 1 or 2 tablets per day for at least 48 weeks

Sponsors

Gunma Liver Study Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Nonalcoholic steatohepatitis (NASH) Resistanace to nutritional treatment or exercise complication with hypertension

Exclusion criteria

Exclusion criteria: Allergy to Angiotensin II receptor Antagonist(ARB) complication with liver diseases due to other causes secondary NASH medication history of ARB or ACE inhibitors

Design outcomes

Primary

MeasureTime frame
transaminase

Secondary

MeasureTime frame
insulin resistance liver histology

Countries

Japan

Contacts

Public ContactKen Sato

Gunma University Graduate School of Medicine Department of Medicine and Molecular Science

satoken@gunma-u.ac.jp027-220-8127

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026