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Saccharomyces boulardii CNCM I-745

Saccharomyces boulardii

Research reviewed: Up until 03/2026

Saccharomyces boulardii (Saccharomyces boulardii CNCM I-745) is a dietary supplement with 10 published peer-reviewed studies involving 452 participants, researched for Antibiotic-Associated Diarrhea, C. difficile Infection, IBS & IBD and 2 more areas.

10
Studies
452
Participants
2002–2025
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Strong Evidence

Antibiotic-Associated Diarrhea

Moderate
2 studies 2 of 2 positive 190 participants 1 human

C. difficile Infection

Moderate
2 studies 2 of 2 positive 129 participants 1 human

IBS & IBD

Strong
3 studies 2 of 3 positive 124 participants

Acute Diarrhea

Weak
1 study 1 of 1 positive 9 participants 0 human

Gut Health & Infections

Moderate
2 studies 1 of 2 positive 0 participants 1 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

6/10
Randomised
4/10
Double-Blind
4/10
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2006)
10
Study 2 (2010)
180
Study 1 (2006)
124
Study 2 (2017)
5
Study 1 (2015)
67
Study 2 (2002)
32
Study 3 (2008)
25
Study 1 (2013)
9

Research Timeline

When the studies were published

1
2002
2
2006
1
2008
1
2010
1
2013
1
2015
1
2017
2
2025

All Studies

Detailed breakdown of each trial. Click to expand.

Antibiotic-Associated Diarrhea

1

To evaluate S. boulardii for prevention of antibiotic-associated diarrhea.

2006 10 participants Various 250-1000 mg/day across studies
Review/Other Positive

Study Type

Meta-analysis

Purpose

To evaluate S. boulardii for prevention of antibiotic-associated diarrhea.

Dose

250-1000 mg/day across studies

Participants

Meta-analysis of 10 RCTs, 3432 patients

Duration

Various

Results

S. boulardii significantly reduced risk of AAD (RR 0.47, 95% CI 0.35-0.63). NNT = 10. Effects were consistent across all antibiotic classes.

How They Measured It

Pooled risk ratios across included RCTs

Read full study
2

To assess S. boulardii for prevention of AAD in hospitalized patients.

2010 180 participants Duration of antibiotic course + 3 days 500 mg twice daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess S. boulardii for prevention of AAD in hospitalized patients.

Dose

500 mg twice daily

Participants

180 hospitalized patients

Duration

Duration of antibiotic course + 3 days

Results

S. boulardii significantly reduced AAD incidence (7.2% vs 14.6% placebo). Duration of diarrhea was also shorter in treated group.

How They Measured It

Incidence and duration of diarrhea

Read full study

C. difficile Infection

1

To evaluate S. boulardii for prevention of recurrent C. difficile infection.

2006 124 participants 4 weeks 1 g/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate S. boulardii for prevention of recurrent C. difficile infection.

Dose

1 g/day

Participants

124 patients with C. difficile infection

Duration

4 weeks

Results

S. boulardii combined with standard antibiotics significantly reduced C. difficile recurrence (34.6% vs 64.7% in high-dose vancomycin subgroup).

How They Measured It

Recurrence rate of C. difficile diarrhea

Read full study
2

To evaluate S. boulardii for prevention and treatment of C. difficile-associated disease.

2017 5 participants Various Various
Review/Other Positive

Study Type

Systematic review and meta-analysis

Purpose

To evaluate S. boulardii for prevention and treatment of C. difficile-associated disease.

Dose

Various

Participants

Meta-analysis of 5 RCTs, 1076 patients

Duration

Various

Results

S. boulardii significantly reduced risk of C. difficile recurrence (RR 0.59, 95% CI 0.41-0.85). Evidence strongest for recurrent C. difficile.

How They Measured It

Pooled risk ratios for recurrence

Read full study

IBS & IBD

1

To evaluate S. boulardii for IBS-D symptoms.

2015 67 participants 4 weeks 750 mg/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate S. boulardii for IBS-D symptoms.

Dose

750 mg/day

Participants

67 IBS-D patients

Duration

4 weeks

Results

S. boulardii significantly improved quality of life scores and reduced stool frequency compared to placebo. Modest improvement in abdominal pain.

How They Measured It

IBS-QoL, stool frequency and consistency, abdominal pain

Read full study
2

To evaluate S. boulardii as adjunct therapy in Crohn's disease.

2002 32 participants 6 months 1 g/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate S. boulardii as adjunct therapy in Crohn's disease.

Dose

1 g/day

Participants

32 patients with Crohn's disease in remission

Duration

6 months

Results

S. boulardii group had significantly lower relapse rate (6.25% vs 37.5% placebo) and maintained lower CDAI scores.

How They Measured It

CDAI, relapse rate

Read full study
3

To assess S. boulardii in ulcerative colitis maintenance therapy.

2008 25 participants 12 months 750 mg/day
Human Study RCT Mixed

Study Type

Randomised controlled trial

Purpose

To assess S. boulardii in ulcerative colitis maintenance therapy.

Dose

750 mg/day

Participants

25 patients with UC in remission

Duration

12 months

Results

S. boulardii as adjunct to mesalamine showed clinical improvement but did not reach statistical significance for relapse prevention compared to mesalamine alone.

How They Measured It

Clinical Activity Index, endoscopic scores, relapse rate

Read full study

Acute Diarrhea

1

To evaluate S. boulardii for treatment of acute diarrhea in children.

2013 9 participants 3-7 days 250-500 mg/day across studies
Review/Other Positive

Study Type

Meta-analysis

Purpose

To evaluate S. boulardii for treatment of acute diarrhea in children.

Dose

250-500 mg/day across studies

Participants

Meta-analysis of 9 RCTs, 1117 children

Duration

3-7 days

Results

S. boulardii significantly reduced duration of acute diarrhea by ~24 hours (WMD −23.1 hours, 95% CI −31.7 to −14.5). Effective in both viral and bacterial diarrhea.

How They Measured It

Duration of diarrhea, stool frequency

Read full study

Gut Health & Infections

4

To evaluate the efficacy and safety of Saccharomyces boulardii combined with standard quadruple therapy for H. pylori eradication in adults.

2025 ? participants Various S. boulardii CNCM I-745 500-1000 mg/day alongside quadruple ...
Review/Other Positive

Study Type

Meta-Analysis

Purpose

To evaluate the efficacy and safety of Saccharomyces boulardii combined with standard quadruple therapy for H. pylori eradication in adults.

Dose

S. boulardii CNCM I-745 500-1000 mg/day alongside quadruple therapy

Participants

Meta-analysis of adults with H. pylori infection

Duration

Various

Results

S. boulardii addition to quadruple therapy significantly improved eradication rates and reduced adverse effects, particularly diarrhea.

How They Measured It

H. pylori eradication rates, adverse effects (diarrhea, nausea, taste disturbance)

Read full study
5

To evaluate combination therapy of rifaximin and Saccharomyces boulardii CNCM I-745 for small intestinal bacterial overgrowth.

2025 ? participants 4 weeks S. boulardii CNCM I-745 500 mg twice daily plus rifaximin
Human Study RCT Mixed

Study Type

Randomized Controlled Trial

Purpose

To evaluate combination therapy of rifaximin and Saccharomyces boulardii CNCM I-745 for small intestinal bacterial overgrowth.

Dose

S. boulardii CNCM I-745 500 mg twice daily plus rifaximin

Participants

Patients with SIBO associated with PPI use

Duration

4 weeks

Results

Combined rifaximin and S. boulardii therapy showed superior SIBO eradication rates and symptom improvement compared to rifaximin alone.

How They Measured It

SIBO breath test results, symptom scores, gut microbiome markers

Read full study

Frequently Asked Questions

Common questions about Saccharomyces boulardii research

What does the research say about Saccharomyces boulardii?

There are currently 10 peer-reviewed studies on Saccharomyces boulardii (Saccharomyces boulardii CNCM I-745), involving 452 total participants. Research covers Diarrhea prevention, C. difficile infection, IBD support and 1 more areas. The overall evidence strength is rated as Strong.

How strong is the evidence for Saccharomyces boulardii?

The evidence is currently rated as "Strong Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (6 human studies), and reported outcomes.

What health goals has Saccharomyces boulardii been studied for?

Saccharomyces boulardii has been researched for: Diarrhea prevention, C. difficile infection, IBD support, Gut health. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Saccharomyces boulardii based on human trials?

Yes, 6 out of 10 studies are human trials. Human trials carry more weight in our evidence scoring system.