Actively Recruiting
The Effects of Antrodia Cinnamomea Fruiting Body Extract on Quality of Life and Chemotherapy Side Effects in Patients With Lung Cancer Undergoing Platinum-Based Chemotherapy
Led by Tri-Service General Hospital · Updated on 2026-01-08
40
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
T
Tri-Service General Hospital
Lead Sponsor
B
Balay Biotechnology Corporation
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating whether a nutritional supplement called Antrodia cinnamomea can improve quality of life for lung cancer patients receiving platinum-based chemotherapy. Lung cancer patients often face side effects like nausea, vomiting, sleep problems, and other symptoms during chemotherapy. This study aims to see if adding Antrodia cinnamomea to turmeric and probiotics can help reduce these side effects and improve overall well-being. Participants will be randomly assigned to one of two groups: one group will take capsules containing Antrodia cinnamomea extract combined with turmeric and probiotics, and the other group will take capsules with turmeric and probiotics only. Both groups will take their assigned capsules orally once daily for 3 months while undergoing chemotherapy. After this, researchers will follow participants for an additional 3 months (up to 24 weeks total) to observe lasting effects of the supplement. During the study, participants will complete questionnaires at multiple timepoints to assess nausea and vomiting, sleep quality, cancer symptoms, and overall quality of life. Researchers will also measure skeletal muscle mass. These assessments will occur at baseline and various weeks during and after treatment. The study is double-blind and randomized, ensuring neither participants nor doctors know which capsules are taken. Total participation lasts about 6 months with regular monitoring.
CONDITIONS
Brief Title
Antrodia Cinnamomea Extract Effects on Lung Cancer Patients' Quality of Life During Chemotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pathologically and radiographically diagnosed lung cancer
- Age greater than 18 years
- Receiving platinum-based chemotherapy
- Life expectancy of six months or longer
You will not qualify if you...
- Unable to comply with timely supplement administration
- Abnormal liver or kidney function within 14 days prior to entry
- Unexplained fever ≥38.5°C for 7 consecutive days or chronic diarrhea for 15 consecutive days within 30 days prior to entry
- Currently receiving hormone therapy
- Major cardiac disease or arrhythmia deemed unsuitable by physician
- Major neuropathy
- Active acute infections
- Known allergies to study product or ingredients
- Currently taking supplements containing Antrodia camphorata extract
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 months
Participants take daily capsules containing either Antrodia cinnamomea combined with turmeric and probiotics or turmeric and probiotics alone during their platinum-based chemotherapy treatment.
Regular assessments at Baseline, Week 3, and Week 12
Duration - 3 months
Researchers continue to monitor participants for lasting effects of the supplement through questionnaires assessing nausea, vomiting, sleep quality, symptoms, and quality of life.
Assessments at Week 18 and Week 24
Trial Site Locations
Total: 1 location
1
Tri-Service General Hospital
Taipei, Taiwan, 114
Actively Recruiting
Research Team
C
Chen-Liang Tsai
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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