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Effect of TCI188 Probiotic on Oral Health

T

TCI

Status

Completed

Conditions

Periodontal Diseases

Treatments

Dietary Supplement: Placebo
Dietary Supplement: TCI188 Probiotic

Study type

Interventional

Funder types

Industry

Identifiers

NCT06141083
N202307006

Details and patient eligibility

About

To assess the efficacy of TCI188 (Pediococcus acidilactici) Probiotic on Oral Health

Enrollment

55 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female over 18 years old
  • Participants suffer from severe periodontal disease throughout the mouth with symptoms at third and fourth stages, do not have immediate indications for the extraction of multiple teeth or complex denture stimulation, and have not undergone periodontal planing within one year.

Exclusion criteria

  • Participants have had periodontal or antimicrobial treatment within the past 6 months
  • Participants are smokers, pregnant or with systemic diseases
  • Participants had probiotic supplements or with history of adverse reactions to lactose or fermented dairy products

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

55 participants in 2 patient groups, including a placebo group

Placebo chewable tablets
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo
TCI188 Probiotic chewable tablets
Experimental group
Treatment:
Dietary Supplement: TCI188 Probiotic

Trial contacts and locations

1

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Central trial contact

Chin-Wei Wang; Ping Lin

Data sourced from clinicaltrials.gov

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