Actively Recruiting

Phase Not Applicable
Age: 20Years - 80Years
All Genders
NCT06039644

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

Age: 20Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Mackay Memorial Hospital

Taipei, Taiwan

Actively Recruiting

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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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To Evaluate the Clinical Efficacy of Probiotics in Patients With the Breast Cancer | DecenTrialz