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Completed

NCT Number: NCT04754464

Clinical Study on the Effect of a Synbiotic on Body Fat Mass

In this trial the effect of a synbiotic consisting of the three different strains of Lactobacillus fermentum and acacia gum (gum arabic) on body fat mass, body weight, long-term glycemia, insulin resistance and other risk factors for CVD and diabetes in overweight type 2 diabetics is investigated.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Slimbiotics GmbH, Vienna, Austria

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About this study

The effects of probiotics on glucose and lipid metabolism, on body fat, weight, visceral fat and liver steatosis were shown by several meta-analyses for the total variety, as described above. Some probiotic species/strains, however, seem to be more efficacious. The lactobacilli used in this trial were selected for their anti-inflammatory properties and based on induction of defensins in enterocytes. Therefore, one may expect more pronounced effects of these strains on traits of the metabolic syndrome, which is driven by low grade inflammation, than those found in the meta-analyses for the whole variety of probiotics without discriminating species and strain specificity.

The combination of these Lactobacillus strains with acacia gum is expected to enable even more pronounce effects, since acacia gum was shown to increase the number of lactobacilli in the gut and, hence, are supposed to promote their propagation and, hence their effects. The dosage of 10 g/day acacia gum was demonstrated to be sufficient for enhancing fecal lactobacilli and bifidobacterial.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Overweight or obese (BMI ≥ 25)
  • Type 2 diabetes
  • Age ≥ 18
  • Written informed consent

Exclusion criteria

Any of the following is regarded as a criterion for exclusion from enrollment into the study:

  • Subjects currently enrolled in another clinical study
  • Subjects having finished another clinical study within the last 4 weeks before inclusion
  • Hypersensitivity, allergy or intolerance against any compound of the test products (e. g. acacia gum)
  • Condition after implantation of a cardiac pacemaker or other active implants
  • Antidiabetic drugs except metformin
  • Any disease or condition which might compromise significantly the hepatic (ascites), hematopoietic, renal, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal or any other body system with the exception of the conditions defined by the inclusion criteria
  • History of hepatitis B, C, HIV
  • History of or present liver deficiency as defined by Quick < 70%
  • Regular medical treatment including OTC, which may have impact on the study aims (e.g. probiotics containing supplements etc.)
  • Major cognitive or psychiatric disorders
  • Subjects who are scheduled to undergo any diagnostic intervention or hospitalization which may cause protocol deviations
  • Simultaneous study participation by members of the same household
  • Pregnancy and lactation
  • Any diet to lose body weight
  • Eating disorders or vegan diet
  • Anorexic drugs and laxatives
  • Present drug abuse or alcoholism
  • Legal incapacity

Treatment and study plan

Synbiotic

Dietary Supplement

Consumption of 6 g powder consisting of the strains Lactobacillus fermentum K7-Lb1, L. fermentum K8-Lb1, L. fermentum K11-Lb3, acacia gum (gum arabic), maltodextrin, sucralose and flavour twice a day resolved in water

microcrystalline cellulose

Dietary Supplement

Consumption of 6 g powder containing microcrystalline cellulose, maltodextrin , sucralose and flavour twice a day, resolved in water

Primary outcomes

  1. BFM

    Time frame: 12 weeks

    Body Fat Mass (BFM) as assessed by bioelectrical impedance analysis (BIA) (alteration V3-V1; verum versus placebo group)

Secondary outcomes

  1. HbA1c

    Time frame: 12 weeks

    Glycated Hemoglobin

  2. HOMA-IR

    Time frame: 12 weeks

    HOMA-IR (Homeostasis Model Assessment (HOMA)-IR = glucose [mmol/L] x insulin [µU/ml]/22,5) as parameter for insulin resistance

Other outcomes

  1. WC

    Time frame: 12 weeks

    Waist Circumference

  2. WHtR

    Time frame: 12 weeks

    waist-to-height ratio

Sponsors and collaborators

Lead sponsor

Slimbiotics GmbH

Industry

Collaborators

  • Clinical Research Center Kiel GmbH

Registry information

Official study title

Randomised, Controlled, Double-blind Clinical Study on the Effect of a Synbiotic on Body Fat Mass, Weight Management, Metabolic Syndrome and Other Risk Factors for CVD and Diabetes, on Fecal Microbiota and Adverse Effects

Important dates

Study start
2020
Primary completion
2021
Study completion
2022
First posted
Feb 15, 2021
Registry last updated
Jun 1, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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