Taiwan Green Propolis for Blood Lipids and Body Fat in Patients With MASLD
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Metabolic Dysfunction-Associated Steatotic Liver Disease, Non-alcoholic Fatty Liver Disease NAFLD, Dyslipidemia, Obesity & Overweight
In brief
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.
Key facts
- Study ID
- NCT07692438
- Run by
- Taipei Medical University
- People needed
- 60
- Starts
- 2025-05-28
- Expected to finish
- 2028-09-30
- Last updated by the study team
- 2026-07-09
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Known allergy to honey, propolis, multiple pollens, or alcohol
- Psychiatric disorder or cognitive impairment
- Currently pregnant or breastfeeding
- Significant endocrine abnormality, or major disease of the heart, liver (other than MASLD), or kidney
- Difficulty swallowing capsules
- Dementia, impaired consciousness, or inability to respond to questionnaires
Where it is running
- Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation — Dalin, Taiwan (enrolling)
Full record on ClinicalTrials.gov
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