ClinicalTrials.Veeva

Menu

Antiviral Activity of Oral Probiotics

J

John Hale

Status

Unknown

Conditions

Lower Respiratory Tract Infection
Upper Respiratory Tract Infection

Treatments

Dietary Supplement: Streptococcus salivarius M18 Powder (1 Billion colony forming units /g) with a prebiotic included
Dietary Supplement: Streptococcus salivarius K12 Powder 1 Billion colony forming units /g)
Dietary Supplement: Streptococcus salivarius M18 Powder (1 Billion colony forming units /g)
Dietary Supplement: Streptococcus salivarius K12 Powder (1 Billion colony forming units /g) with a prebiotic included

Study type

Interventional

Funder types

Industry

Identifiers

NCT05374070
BLTCT2022/2

Details and patient eligibility

About

The aim of this study is to test saliva samples obtained from healthy human participants for anti-viral activity after they have consumed S. salivarius probiotic in a powder format.

Full description

This is a randomized controlled open pilot study to evaluate saliva samples collected from participants following their consumption of powders containing the commercially marketed probiotic bacterium S. salivarius K12 or S. salivarius M18.

Participants will be randomly assigned to one of the 4 groups consuming probiotic powder containing Streptococcus salivarius K12 or S. salivarius M18 with or without prebiotics (e.g. sugars that may promote probiotic activity). Saliva samples will be collected at predetermined time points pre and post intervention. Antibacterial and Antiviral activity will be determined following established assays. Colonisation efficacy will be determined by enumerating the probiotic in the saliva samples using standard microbiological techniques.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. In general good health 18 - 80 years of age.
  2. Practice good oral hygiene.

Exclusion criteria

  1. Have a history of autoimmune disease or are immunocompromised.
  2. Are on concurrent antibiotic therapy or regular antibiotic use within last 1 week
  3. History of allergy (e.g. dairy).

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 4 patient groups

Streptococcus salivarius K12
Active Comparator group
Description:
Streptococcus salivarius K12 (Dose 1: 1 Billion colony forming units /g)
Treatment:
Dietary Supplement: Streptococcus salivarius K12 Powder 1 Billion colony forming units /g)
Streptococcus salivarius K12 with a prebiotic included
Active Comparator group
Description:
Streptococcus salivarius K12 (Dose 1: 1 Billion colony forming units /g)
Treatment:
Dietary Supplement: Streptococcus salivarius K12 Powder (1 Billion colony forming units /g) with a prebiotic included
Streptococcus salivarius M18
Active Comparator group
Description:
Streptococcus salivarius M18 (Dose 1: 1 Billion colony forming units /g)
Treatment:
Dietary Supplement: Streptococcus salivarius M18 Powder (1 Billion colony forming units /g)
Streptococcus salivarius M18 with a prebiotic included
Active Comparator group
Description:
Streptococcus salivarius M18 (Dose 1: 1 Billion colony forming units /g)
Treatment:
Dietary Supplement: Streptococcus salivarius M18 Powder (1 Billion colony forming units /g) with a prebiotic included

Trial contacts and locations

1

Loading...

Central trial contact

John D Hale, PhD; John R Tagg, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems