Actively Recruiting
To Evaluate the Clinical Efficacy of Probiotics in Patients With the Breast Cancer
Led by GenMont Biotech Incorporation · Updated on 2026-03-06
100
Participants Needed
1
Research Sites
142 weeks
Total Duration
On this page
Sponsors
G
GenMont Biotech Incorporation
Lead Sponsor
M
Mackay Memorial Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Chemotherapy-associated side-effects would affect therapeutic effect, quality of life, and cause permanent harm to breast cancer patients. This study is designed to explore after consumption of probiotics of lactobacillus composite strain powder sachets for 6 months in breast cancer chemotherapy, and whether the improvement of meliorate the side effects, further assists patients completing the chemotherapy.
CONDITIONS
Official Title
To Evaluate the Clinical Efficacy of Probiotics in Patients With the Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Stage I-III breast cancer patients using anthracycline-based or taxane-based chemotherapy (before or after chemotherapy/surgery)
- Body mass index (BMI) greater than 18 kg/m²
- Age between 20 and 80 years old
- Patients judged by physicians to be eligible and willing to participate
You will not qualify if you...
- Pregnant or breastfeeding women
- Patients with history of bariatric surgery, gastrointestinal resections, Crohn's disease, or celiac disease
- Body mass index (BMI) less than 18 kg/m²
- Patients with severe allergy to soybeans or peanuts
- Patients under 20 years old or over 80 years old
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mackay Memorial Hospital
Taipei, Taiwan
Actively Recruiting
Research Team
F
Fang-Kuei Lin, Master
CONTACT
W
Wan-Hua Tsai, PhD
CONTACT
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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