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Prevention for the Development of Liver Tumorigenesis by the Oral Supplementation of Branched-chain Amino Acids

The Evaluation About the Prevention for the Development of Liver Tumorigenesis by the Oral Supplementation of Branched-chain Amino Acids

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01434524
Enrollment
56
Registered
2011-09-15
Start date
2007-04-30
Completion date
2011-06-30
Last updated
2011-09-15

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

Conditions

Liver Cancer

Brief summary

The long-term outcomes of branched-chain amino acid (BCAA) administration in patients undergoing hepatic resection remain unclear. The aim of this study is to assess the impact of oral supplementation with BCAA on the prevention for the development of liver tumorigenesis in patients undergoing liver resection.

Detailed description

This study might demonstrate a tendency of the improvement in the cumulative tumor recurrence rate after hepatectomy for liver neoplasm in the Livact group compared to that in the Control Group. The investigators believe that BCAA seems to be a remarkable benefit for liver resection, especially on its reduction in the recurrence of liver cancer. This treatment regimen has potential to offer benefits for clinical use selectively, especially for patients with chronic liver diseases.

Interventions

DRUGLIVACT

LIVACT contains 13.0 g of free amino acids

Sponsors

Kochi University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* These patients were scheduled for elective liver resection to treat hepatocellular carcinoma or adenocarcinoma of the liver.

Exclusion criteria

* a body-weight loss greater than 10% during the 6 months prior to surgery, * the presence of distant metastases, or * serious impairment of organ function due to respiratory, renal, or heart disease.

Design outcomes

Primary

MeasureTime frame
Postoperative tumor recurrence rate5 years follow up

Secondary

MeasureTime frameDescription
nutritional status5 years follow upThe secondary endpoint was a comparison of measurements of body weight, arm muscle circumference (AMC) between patient groups.

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026