ClinicalTrials.Veeva

Menu

Evaluation of the Alcohol Elimination Effect of TCI711 Probiotic (Bacillus Coagulans) on Adult Individuals

T

TCI

Status

Completed

Conditions

Breath Alcohol Level

Treatments

Dietary Supplement: Bacillus coagulans TCI711

Study type

Interventional

Funder types

Industry

Identifiers

NCT04457661
20-036-A

Details and patient eligibility

About

Investigating the possibility of using Bacillus coagulans TCI711 to improve the efficiency of alcohol removal in adult individuals.

Enrollment

19 patients

Sex

All

Ages

20 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers aged between 20 to 60.
  • Systolic pressure below 140
  • Score of C-CAGE Questionnaire below 8 (male)/6 (female)
  • Prohibiting other supplements before 2 weeks of the study and during the study
  • Prohibiting alcohol drinks before 24 hours of the study
  • Prohibiting caffeine drinks before 12 hours of the study

Exclusion criteria

  • Alcohol or drug allergy
  • Liver, kidney, cardiovascular, or chronic diseases
  • Other severe disorders
  • Hypertension
  • Pregnancy or lactation
  • Already involved in clinical testing
  • Other supplements

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

19 participants in 1 patient group

TCI711 probiotic
Experimental group
Description:
Taking one capsule (containing 10\^10 of Bacillus coagulans TCI711) daily for one month
Treatment:
Dietary Supplement: Bacillus coagulans TCI711

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems