None listed
Conditions
Interventions
1 capsule containing 1 billion per day of Lactobacillus fermentum PCC daily for 77 days
Sponsors
Probiomics Ltd
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
Inclusion to the study will be determined according to physical activity levels with subjects required to be undertaking 3 exercise sessions weekly and a questionnaire to determine subject’s health in the previous month
Exclusion criteria
Use of immunomodulatory medications, asthma, GI illness
Outcome results
None listed