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Tolerability and Risk of Adverse Events With a Probiotic Supplement

Tolerability and Risk of Adverse Events With a Probiotic Supplement: A Randomised and Placebo Controlled Study in Healthy Individuals

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03728868
Enrollment
50
Registered
2018-11-02
Start date
2018-10-10
Completion date
2019-05-31
Last updated
2020-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Individuals

Keywords

Faecalibacterium prausnitzii, Desulfovibrio piger, tolerability, blood glucose levels

Brief summary

The butyrate-producing bacterium Faecalibacterium prausnitzii is abundant in the human bowel and can make up to 5% of the gastrointestinal flora in healthy individuals. A reduced presence of it has been associated with an imbalance in the gastrointestinal flora of metabolic syndromes such as type 2 diabetes, fat liver, and in inflammatory bowel disease. The present double-blind, placebo-controlled, randomized study is designed to investigate if dietary supplementation with F.prausnitzii (combined with D. piger) once a day for 8 consecutive weeks is tolerated compared to placebo and if it can affect the metabolism in a positive way.

Detailed description

The understanding of the role of the gastrointestinal microbes for human health has gained considerable interest in recent years. The butyrate-producing bacterium Faecalibacterium prausnitzii is a naturally occurring bacterial species in the human gut that can make up to 5% of the gastrointestinal flora in healthy individuals. Several studies have shown that the presence of butyrate producing bacteria, including F. prausnitzii, is lower in patients with inflammatory bowel disease; Crohn's disease and ulcerative colitis. Furthermore, lower levels of short fatty acids have been found in people with ulcerative colitis as compared to healthy individuals. Similar results have been obtained from studies about Crohn's disease, where people with a low abundance of F. prausnitzii run a higher risk of post-operative recurrence of their disease. It has become evident that bacteria in the human gastrointestinal tract are symbiotic and dependent on each other's metabolism. Studies conducted by the sponsor (Metabogen AB) have shown that butyrate production from F. prausnitzii increases in the presence of Desulfovibrio piger, a common sulphate-reducing bacterium present in the human intestine. The symbiotic relationship between F. prausnitzii and D. piger can be utilised by combining these bacterial species into a probiotic dietary supplement, thus maintaining butyrate production in the intestine. In animal models, who received approximately 5,000 times higher doses per kilogram of body weight than the highest dose scheduled in the proposed study, the intake of F. prausnitzii has shown anti-inflammatory effects as well as positive effects on the metabolism. The present study is a double-blind, placebo-controlled, randomized, study in 48 healthy individuals (men and women) between 20 and 40 years old recruited from the general population. These volunteers will either receive F. prausnitzii and D. piger (in two different doses) or placebo orally once a day for 8 consecutive weeks. The investigators will assess how well treatment with the study product compared to placebo is tolerated (termination due to adverse events within 8 weeks of treatment) and if it can cause gastrointestinal symptoms (measured with The Gastrointestinal Symptom Rating Scale). The investigators will also assess if the intake of the study product can potentially give positive effects in the metabolism (blood glucose, fatty acids, protein ect).

Interventions

DIETARY_SUPPLEMENTPlacebo

Dietary supplementation with placebo once a day for 8 consecutive weeks

DIETARY_SUPPLEMENTHigh dose F. prausnitzii and D. piger

Dietary supplementation with high dose F. prausnitzii and D. piger once a day for 8 consecutive weeks

DIETARY_SUPPLEMENTLow dose F. prausnitzii and D. piger

Dietary supplementation with low dose F. prausnitzii and D. piger once a day for 8 consecutive weeks

Sponsors

MetaboGen AB
CollaboratorINDUSTRY
Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

1. 20 to 40 years old 2. Signed consent for participation 3. Healthy individuals without any known diseases 4. Willingness and ability to attend to planned visits, participate in telephone interviews and follow study instructions 5. Understanding the Swedish language in spoken and written terms

Exclusion criteria

1. Ongoing treatment with prescription drugs 2. Regular or sporadic intake of probiotic products (foods with probiotics are allowed) 3. Treated with antibiotics during the last 3 months 4. Pregnancy 5. Have experienced gastrointestinal tract symptoms (during the last month), which could affect study participation, as deemed by study physician. 6. Current tobacco use (smoking or snuff) 7. Participation in another clinical study

Design outcomes

Primary

MeasureTime frameDescription
Tolerability of the oral intake of F. prausnitzii and D. piger, defined as study discontinuation due to adverse events under 8 weeks of treatment.0-8 weeksHow well treatment with the study product compared to placebo is tolerated, which is primarily defined as termination due to adverse events under 8 weeks of treatment.

Secondary

MeasureTime frameDescription
Effects on inflammation - erythrocyte sedimentation rate (safety parameters )0-8 weeksChange in erythrocyte sedimentation rate in blood. Significant change in erythrocyte sedimentation rate before and after the 8-week treatment period.
Effects on inflammation - CRP (safety parameters )0-8 weeksChange in C-reactive protein (CRP) level in blood. Significant change in CRP before and after the 8-week treatment period.
Effect on hematopoiesis - red blood cells (safety parameters)0-8 weeksChanges in red blood cells count. Significant change in red blood cell count before and after the 8-week treatment period.
Effect on hematopoiesis - white blood cells (safety parameters)0-8 weeksChanges in white blood cells count. Significant change in white blood cells count before and after the 8-week treatment period.
Effect on hematopoiesis - platelets (safety parameters)0-8 weeksChanges in platelets count. Significant change in platelets count before and after the 8-week treatment period.
Effects on liver enzymes - ALAT (safety parameters)0-8 weeksChanges in liver enzyme ALAT (Alanine transaminase). Significant changes before baseline and after 8 weeks of treatment.
Effects on liver enzymes - ASAT (safety parameters)0-8 weeksChanges in liver enzyme ASAT (Aspartate transaminase). Significant changes before baseline and after 8 weeks of treatment.
Gastrointestinal side effects, measured using the Gastrointestinal Symptom Rating Scale (GSRS)0-8 weeksGastrointestinal symptoms are measured with The Gastrointestinal Symptom Rating Scale (GSRS), which includes 15 items combined into five symptom clusters measuring 1) reflux, 2) abdominal pain, 3) indigestion, 4) diarrhoea and 5) constipation. GSRS has a seven-point graded Likert-type scale, in which 1 represents absence of troublesome symptoms and 7 represents very troublesome symptoms. The total score is derived from all subclasses, resulting in a score between 0 and 45.
Effects on serum bilirubin (safety parameters)0-8 weeksChanges in serum bilirubin. Significant changes before baseline and after 8 weeks of treatment.
Effects on the blood glucose0-8 weeksChanges (in percent) in levels of fasting blood glucose and HbA1c before and after the 8 week treatment period.
Effects on abundance of short-chain fatty acids0-10 weeksChanges in short-chain fatty acids in stool from baseline to week 10.
Colonization with F. prausnitzii0-8 weeksColonization of the intestine with the total amount of F. prausnitzii bacteria. Measured in stool.
Effect on renal function(safety parameter)0-8 weeksChange in calculated eGFR (Glomerular Filtration Rate, based on serum creatinine)
Effect on serum total protein (safety parameter)0-8 weeksChange in serum total protein
Effects on liver enzymes - ALP (safety parameters)0-8 weeksChanges in liver enzyme, ALP (Alkaline phosphatase). Significant changes before baseline and after 8 weeks of treatment.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026