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A controlled trial of zinc supplementation for decompensated liver cirrhosis

A controlled trial of zinc supplementation for decompensated liver cirrhosis - A controlled trial of zinc supplementation for decompensated LC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000276
Enrollment
90
Registered
2008-01-01
Start date
2005-12-01
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

decompensated liver cirrhosis

Interventions

oral zinc supplementation + BCAA granule only BCAA granule

Sponsors

NHO IwakuniClinical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Decompensated liver cirrhosis more than 12 weeks during BCAA granule administration,and hyperammonemia(more than 50 micromol/l). 2.hepatic encephalopathy is present. or the anamnestic patient (decompensated liver cirrhosis). 3.The prognosis obtained more than one year. 4.Age is within 20-80 years old 5.For patients with HCC the Milan criteria are applied (solitary tumor of less than 5 cm, or three or fewer lesions, none more than 3 cm without vascular invasion, or extrahepatic metastasis), and patients were to undergo potentially curative treatments with percutaneous ethanol injection therapy, combined with transcatheter arterial embolization, radiofrequency ablation therapy, or surgical resection. 6.We do not ask whether hospitalization or outpatient. 7.The patient is obtained an agreement by a document.

Exclusion criteria

Exclusion criteria: 1.The patient with pregnancy or gravid possibility. 2.Advanced HCC, or other malignancy, its prognosis is less than 1 year. 3.Less than 2.5g/ml of serum albumin level 4.More than 3.0mg/dl of total bil. 5.Hepatic encephalopathy (possible anamnestic case) is higher than 3 degree. 6. The patients whom judged to be inadequate by clinical trial liability or clinical trial allotment doctor.

Design outcomes

Primary

MeasureTime frame
QOL(SF-36)

Countries

Japan

Outcome results

None listed

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