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Lacticaseibacillus rhamnosus GG

Lactobacillus rhamnosus GG

Research reviewed: Up until 03/2026

Lactobacillus rhamnosus GG (Lacticaseibacillus rhamnosus GG) is a dietary supplement with 8 published peer-reviewed studies involving 1,965 participants, researched for Diarrhea Prevention & Treatment, IBS & Gut Health, Immune Function.

8
Studies
1,965
Participants
2001–2019
Research Span

Evidence at a Glance

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

Overall: Strong Evidence

Diarrhea Prevention & Treatment

Moderate
3 studies 2 of 3 positive 822 participants 2 human

IBS & Gut Health

Strong
2 studies 2 of 2 positive 245 participants

Immune Function

Moderate
3 studies 1 of 3 positive 898 participants 2 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

6/8
Randomised
4/8
Double-Blind
4/8
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2001)
63
Study 2 (2002)
188
Study 3 (2007)
571
Study 1 (2015)
104
Study 2 (2010)
141
Study 1 (2001)
571
Study 2 (2005)
315
Study 3 (2019)
12

Research Timeline

When the studies were published

2
2001
1
2002
1
2005
1
2007
1
2010
1
2015
1
2019

All Studies

Detailed breakdown of each trial. Click to expand.

Diarrhea Prevention & Treatment

1

To evaluate probiotics for prevention and treatment of acute infectious diarrhea in children.

2001 63 participants Various Various LGG doses (5-40 billion CFU/day)
Review/Other Positive

Study Type

Cochrane systematic review

Purpose

To evaluate probiotics for prevention and treatment of acute infectious diarrhea in children.

Dose

Various LGG doses (5-40 billion CFU/day)

Participants

Systematic review of 63 trials, >8000 participants

Duration

Various

Results

LGG significantly reduced duration of diarrhea by approximately 1 day and reduced risk of diarrhea lasting ≥4 days. Effects were most pronounced in children.

How They Measured It

Duration and severity of diarrhea episodes

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2

To evaluate LGG for prevention of antibiotic-associated diarrhea in children.

2002 188 participants Duration of antibiotic course 10 billion CFU/day
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate LGG for prevention of antibiotic-associated diarrhea in children.

Dose

10 billion CFU/day

Participants

188 children aged 6 months to 10 years

Duration

Duration of antibiotic course

Results

LGG significantly reduced the incidence of antibiotic-associated diarrhea (5% vs 16% placebo, p<0.05).

How They Measured It

Incidence of diarrhea during antibiotic treatment

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3

To assess LGG for treatment of acute gastroenteritis in European children.

2007 571 participants 5 days treatment 10 billion CFU twice daily
Human Study RCT Mixed

Study Type

Multi-center randomised controlled trial

Purpose

To assess LGG for treatment of acute gastroenteritis in European children.

Dose

10 billion CFU twice daily

Participants

571 children with acute gastroenteritis

Duration

5 days treatment

Results

LGG reduced the duration of diarrhea by approximately 24 hours compared to placebo. Hospital stay was also shorter in the LGG group.

How They Measured It

Duration of diarrhea, hospitalization length

Read full study

IBS & Gut Health

1

To evaluate LGG for symptom relief in irritable bowel syndrome.

2015 104 participants 8 weeks 6 billion CFU twice daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate LGG for symptom relief in irritable bowel syndrome.

Dose

6 billion CFU twice daily

Participants

104 IBS patients

Duration

8 weeks

Results

LGG significantly reduced abdominal distension and improved stool consistency. Moderate improvements in overall IBS symptoms were noted.

How They Measured It

IBS symptom scores, abdominal pain frequency

Read full study
2

To assess efficacy of LGG in functional abdominal pain in children.

2010 141 participants 8 weeks 10 billion CFU twice daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess efficacy of LGG in functional abdominal pain in children.

Dose

10 billion CFU twice daily

Participants

141 children aged 5-14 years with functional abdominal pain

Duration

8 weeks

Results

LGG significantly reduced frequency and intensity of abdominal pain episodes compared to placebo. Treatment success rate was 72% vs 53% placebo.

How They Measured It

Pain intensity (Wong-Baker FACES), frequency of pain episodes

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Immune Function

1

To evaluate the effect of LGG on incidence and severity of respiratory infections in children attending daycare.

2001 571 participants 7 months 10 billion CFU/day in milk
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate the effect of LGG on incidence and severity of respiratory infections in children attending daycare.

Dose

10 billion CFU/day in milk

Participants

571 children aged 1-6 in daycare centers

Duration

7 months

Results

LGG reduced the incidence of respiratory infections by 17% and reduced antibiotic treatments by 19% compared to placebo.

How They Measured It

Incidence of respiratory infections, days absent from daycare

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2

To assess LGG supplementation on immune response and infection rates in preterm infants.

2005 315 participants Until discharge 1 billion CFU/day
Human Study RCT Positive

Study Type

Randomised controlled trial

Purpose

To assess LGG supplementation on immune response and infection rates in preterm infants.

Dose

1 billion CFU/day

Participants

315 preterm infants

Duration

Until discharge

Results

LGG supplementation significantly reduced the incidence of NEC stage ≥2 and late-onset sepsis in preterm infants.

How They Measured It

Incidence of necrotizing enterocolitis (NEC), sepsis

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3

To review evidence on LGG for prevention of infections in children.

2019 12 participants Various Various
Review/Other Mixed

Study Type

Systematic review

Purpose

To review evidence on LGG for prevention of infections in children.

Dose

Various

Participants

Review of 12 RCTs

Duration

Various

Results

Moderate evidence supporting LGG for reduction in respiratory and gastrointestinal infections in children, with strongest evidence for daycare settings.

How They Measured It

Pooled analysis across included studies

Read full study

Frequently Asked Questions

Common questions about Lactobacillus rhamnosus GG research

What does the research say about Lactobacillus rhamnosus GG?

There are currently 8 peer-reviewed studies on Lactobacillus rhamnosus GG (Lacticaseibacillus rhamnosus GG), involving 1,965 total participants. Research covers Diarrhea prevention, Gut health, Pediatric GI health and 1 more areas. The overall evidence strength is rated as Strong.

How strong is the evidence for Lactobacillus rhamnosus GG?

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 Lactobacillus rhamnosus GG been studied for?

Lactobacillus rhamnosus GG has been researched for: Diarrhea prevention, Gut health, Pediatric GI health, Immune support. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Lactobacillus rhamnosus GG based on human trials?

Yes, 6 out of 8 studies are human trials. Human trials carry more weight in our evidence scoring system.