Research on the Improvement of Intestinal and Immune Functions by Probiotics

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorWecare Probiotics Co., Ltd.

About this trial

Evaluate the effectiveness and safety of Limosilactobacillus fermentum LF61 as a food supplement compared to a placebo in improving intestinal and immune functions in healthy adults.

Eligibility criteria

Qualifiers

Willing to undergo 3 follow-up visits during the intervention period

Be willing to provide blood, urine and stool samples 2 times during the intervention period

Willing to self-administer one of the 7 probiotics (BI45, BBi32, LS97, LB42, LF61, LH76, LR08)/placebo once a day during the intervention period

Good eyesight, can read and write, can wear glasses

Disqualifiers

Digestive diseases, mainly gastrointestinal diseases (celiac disease, ulcerative colitis, Crohn's disease)

Have a serious neurological condition (epilepsy, stroke, severe head trauma, meningitis in the last 10 years, brain surgery, brain tumor, prolonged coma - not including general anaesthesia)

Have received/are receiving treatment for the following mental disorders: alcohol/drug/substance abuse dependence, schizophrenia, psychosis, bipolar disorder

Take medication for depression or low mood

Trial design

Treatments tested in this trial

  • Probiotic
  • Placebo

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators