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NCT Number: NCT07143955

Dietary Intervention and Gut Microbiota in Hepatocellular Carcinoma (HCC)

This prospective, randomized controlled trial investigates the efficacy of a targeted dietary intervention in patients with hepatocellular carcinoma (HCC). The study aims to compare a structured diet including probiotics and prebiotics against routine dietary care. The primary goal is to assess the impact on clinical outcomes (survival), gut microbiota composition, systemic lipid metabolism, and anti-tumor immune responses, to determine if this intervention can serve as an effective adjunctive therapy for HCC.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Hospital of Hebei Medical University

Shijiazhuang, Hebei, 050000, China

About this study

Hepatocellular carcinoma (HCC) is associated with gut microbiota dysbiosis, which contributes to a pro-inflammatory and immunosuppressive tumor microenvironment via the "gut-liver axis." This study hypothesizes that modulating the gut microbiota through a targeted dietary intervention can rebalance systemic immunity and improve clinical outcomes. This single-center, prospective trial randomized 100 patients with HCC into two groups. The experimental group (n=50) received a structured dietary plan including high-fiber foods, probiotics (Bifidobacterium, Lactobacillus), and prebiotics. The control group (n=50) received routine dietary counseling. The study evaluates the intervention's effects on progression-free survival (PFS), overall survival (OS), gut microbiota diversity, serum lipid profiles, peripheral immune cell populations (CD8+ T cells, Tregs), and quality of life. The findings aim to provide robust clinical evidence for integrating microbiota-targeted dietary therapy into the standard management of HCC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 80 years.
  • Pathologically confirmed primary Hepatocellular Carcinoma (HCC).
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  • Adequate organ function (e.g., liver, renal, and bone marrow).
  • Life expectancy of at least 3 months.
  • Willingness to provide informed consent and adhere to study procedures.

Exclusion criteria

  • Concurrent malignancies other than HCC.
  • Severe, uncontrolled comorbidities (e.g., congestive heart failure, renal failure).
  • Known history of severe intestinal diseases such as inflammatory bowel disease.
  • Use of antibiotics, probiotics, or other microbiota-altering agents within 4 weeks prior to enrollment.
  • Cognitive impairment precluding understanding of the study.
  • Refusal to provide consent.

Treatment and study plan

Structured Dietary Intervention

Behavioral

A comprehensive dietary program consisting of dietary modification (high-fiber, lean protein), daily probiotic supplementation capsule (Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus), and encouraged intake of prebiotics and unsaturated fatty acids.

Routine Dietary Care

Behavioral

Standard institutional dietary counseling for patients with HCC, providing general advice on nutrition.

Primary outcomes

  1. Progression-Free Survival (PFS)

    Time frame: Through study completion, an average of 12 months

    Defined as the time from randomization to the first documented disease progression or death from any cause, whichever occurred first. Disease progression was assessed according to standard oncologic criteria.

  2. Overall Survival (OS)

    Time frame: Through study completion, an average of 12 months

    Defined as the time from randomization to death from any cause.

Secondary outcomes

  1. Change in Gut Microbiota Alpha-Diversity

    Time frame: Baseline, 12 months

    Measured by the Shannon and Simpson indices from fecal samples using 16S rRNA sequencing.

  2. Change in Gut Microbiota Composition

    Time frame: Baseline, 12 months

    Relative abundance of key bacterial genera (e.g., Bifidobacterium, Lactobacillus, Escherichia coli) assessed by 16S rRNA sequencing.

  3. Change in Serum Lipid Profile

    Time frame: Baseline, 12 months

    Measured levels of serum cholesterol and triglycerides.

  4. Change in Health-Related Quality of Life (QOL)

    Time frame: Baseline, 12 months

    Assessed using the World Health Organization Quality of Life (WHOQOL-100) questionnaire. Scores for each domain range from 4 to 20, with higher scores indicating a better quality of life.

  5. Incidence of Treatment-Related Adverse Events

    Time frame: Throughout the study duration, up to 18 months

    Safety and tolerability assessed by documenting adverse events throughout the study.

Sponsors and collaborators

Lead sponsor

The First Hospital of Hebei Medical University

Other

Registry information

Official study title

A Randomized Controlled Trial of a Targeted Dietary Intervention to Reshape Gut Microbiota and Lipid Metabolism for Enhancing Anti-Tumor Immunity and Prognosis in Patients With Hepatocellular Carcinoma

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Aug 27, 2025
Registry last updated
Aug 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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