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The effect of rifaximin on liver cirrhosis patients with hepatic encephalopathy

The effect of rifaximin on liver cirrhosis patients with hepatic encephalopathy - The effect of rifaximin on liver cirrhosis patients with hepatic encephalopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032548
Enrollment
50
Registered
2018-05-11
Start date
2017-04-01
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

liver cirrhosis

Interventions

Rifaximin 400 mg administered three times a day for 4 weeks.

Sponsors

Nara Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The subjects are patients with decompensated cirrhosis due to several causes, aged 18 years or older, who have been diagnosed by clinical, biochemical, and ultrasound findings.

Exclusion criteria

Exclusion criteria: The exclusion criteria are cardiac and/or respiratory failure or invasive cancer within the past 5 years; renal failure; clinical or biochemical signs of infection 28 d prior to inclusion; concomitant inflammatory bowel diseases and/or irritable bowel syndrome; previous history of gastrectomy, enterectomy, and/or liver transplantation; and developed portosystemic shunt. Patients who consume nonabsorbable disaccharides, probiotics, prebiotics, synbiotics, or other antibiotics 28 days prior to inclusion are also excluded.

Design outcomes

Primary

MeasureTime frame
Effectiveness to hepatic encephalopathy (serum ammonia value, endotoxin activity)

Countries

Japan

Contacts

Public ContactKosuke Kaji

Nara Medical University Third Department of Internal Medicine

kajik@naramed-u.ac.jp0744-22-3051

Outcome results

None listed

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