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RECRUITING
NCT06039644
NA

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

Sponsor: GenMont Biotech Incorporation

View on ClinicalTrials.gov

Summary

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.

Official title: To Evaluate the Efficacy of Probiotics in Improvement and Prevention of Chemotherapy Associated Side Effectes in Patients With the Breast Cancer

Key Details

Gender

All

Age Range

20 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-04-08

Completion Date

2026-12-31

Last Updated

2026-03-06

Healthy Volunteers

No

Conditions

Interventions

DIETARY_SUPPLEMENT

Probiotic

Three-strain probiotic supplement includes Lactobacillus reuteri GMNL-89 (alive), Lactobacillus plantarum GMNL-141 (alive) and Lactobacillus paracasei GMNL-133 (alive).

OTHER

Placebo

Same additives to Probiotic group but replace probiotics with corn starch and Maltodextrin.

Locations (1)

Mackay Memorial Hospital

Taipei, Taiwan