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NCT07692438Recruiting

Taiwan Green Propolis for Blood Lipids and Body Fat in Patients With MASLD

A Double-Blind, Randomized, Placebo-Controlled Trial to Evaluate the Effectiveness of Taiwan Green Propolis Supplementation on Blood Lipids and Body Fat in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Source: ClinicalTrials.gov · Last updated 9 Jul 2026

Brief summary (registry, in English)

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a common chronic liver condition linked to excess body fat, high blood lipids, and other metabolic problems. Taiwan green propolis is a natural health product collected by bees from plants, which has shown potential benefits for blood lipids and body fat in laboratory and animal studies. However, its effects in people with MASLD have not been well established in clinical trials. This study is a double-blind, randomized, placebo-controlled trial enrolling up to 60 adults with MASLD at Dalin Tzu Chi Hospital in Taiwan. Eligible participants are randomly assigned in a 1:1 ratio to receive either Taiwan green propolis capsules or matching placebo capsules for 12 weeks. Participants take 2 capsules before breakfast and 2 capsules before dinner each day (4 capsules per day total). Neither participants nor the research team know which capsules are being taken until the study ends. The study measures changes in blood lipids (triglycerides, total cholesterol, LDL-C, and HDL-C), body fat percentage, body weight, waist circumference, liver enzymes, blood sugar levels, inflammatory markers, and health-related quality of life. Liver fat and scarring are assessed by abdominal ultrasound before and after the intervention. Gut microbiota samples are also collected. Assessments are conducted at baseline, at 4 weeks, 8 weeks, 12 weeks (end of intervention), and at follow-up visits 2 weeks and 12 weeks after the intervention ends. The goal of this study is to provide scientific evidence on whether Taiwan green propolis can safely and effectively improve blood lipids, body fat, and metabolic health in people with MASLD, and to explore the relationship between physiological improvements and health behavior changes.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
27 Jun 2026
Start date
28 May 2025
Primary completion date
30 Sept 2028
Lead sponsor
Taipei Medical University
NCT number
NCT07692438

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 28 May 2025 to the primary completion date, 30 Sept 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known allergy to honey, propolis, multiple pollens, or alcohol
  • Psychiatric disorder or cognitive impairment
  • Significant endocrine abnormality, or major disease of the heart, liver (other than MASLD), or kidney
  • Dementia, impaired consciousness, or inability to respond to questionnaires

Other

  • Currently pregnant or breastfeeding
  • Difficulty swallowing capsules

Who the study is looking for

  • Adults aged 18 to 80 years
  • Diagnosis of hepatic steatosis (fatty liver) confirmed by abdominal ultrasound, PLUS at least one of the following metabolic risk factors:
    • Overweight or obesity: BMI \>= 23 kg/m\^2
    • Elevated waist circumference: \>= 90 cm in men or \>= 80 cm in women (South Asian and Chinese criteria)
    • Dysglycemia or type 2 diabetes: prediabetes (HbA1c 5.7-6.4%, or fasting glucose 100-125 mg/dL, or OGTT 2-hour glucose 140-199 mg/dL) OR type 2 diabetes (HbA1c \>= 6.5%, or fasting glucose \>= 126 mg/dL, or OGTT 2-hour glucose \>= 200 mg/dL, or current pharmacological treatment for type 2 diabetes)
    • Elevated triglycerides: \>= 150 mg/dL or currently on lipid-lowering therapy
    • Low HDL-C: \<= 39 mg/dL in men or \<= 50 mg/dL in women, or currently on lipid-lowering therapy
    • Elevated blood pressure: \>= 130/85 mmHg or currently on antihypertensive treatment

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
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DalinTaiwanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.