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Probiotics for Weight Loss

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Karolinska Institute

Status

Completed

Conditions

Overweight

Treatments

Dietary Supplement: LB001

Study type

Interventional

Funder types

Other

Identifiers

NCT04897698
4-1326/2021

Details and patient eligibility

About

This study will investigate a compound of probiotics and prebiotics in females and males with overweight with the aim to evaluate the effect on weight and metabolic markers.

The design is a three month randomized doubled-blinded, three-armed placebo-controlled trial of probiotics for weight loss. Normal dose (2 capsules á 0.4g per day) doubled dose (4 capsules á 0.4g per day), or placebo.

A second, non-blinded, phase with only the compound of probiotics and prebiotics, with tripple dose (6 capsuled á 0.4g per day), will be performed for individuals who had the compound in the first phase.

Full description

Participants Total number of study participants will be 75-90, consisting of overweight men and women, 18-45 years of age.

Treatment Dietary supplement consisting of probiotic capsules called LB001. It contains strains of pediococcus (Bacterial family of Lactobacillaceae) and saccharomycetes (kingdom of Fungi and the division Ascomycota) with a concentration of 13 millions cfu/g. Other ingredients (including stabilization) include rice bran, vegetable L-Cystein, magnesium salts from vegetable fatty acids. The capsule shell is made of vegetable HydroxyPropylMetylCellulosa (HPMC). Each capsule has a weight of 0.4 gram. The placebo is made of rice flour.

Since one of the inclusion criteria is "willingness to lose weight", all study participants, regardless of randomized treatment, will receive general advice regarding healthy lifestyle habits.

Enrollment

81 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • BMI 26.0 - 29,99 kg/m2
  • 18-45 years old
  • Willingness to lose weight

Exclusion criteria

  • Active weight loss in the last three months
  • The desire for or planned pregnancy upcoming months
  • Chronic somatic diseases that may affect metabolic and/or intestinal function (e.g. diabetes, hypertension, dyslipidemia, Irritable Bowel Disorder (IBD), gluten intolerance, pancreatic dysfunction, other causes of malabsorption, neoplastic disease)
  • Allergies with previous anaphylactic reactions
  • Abdominal surgery six months prior to inclusion
  • Current or history of eating disorders
  • Extreme or unusual diets for the last three months, which the investigator considers could negatively affect the outcome of the study
  • Psychiatric disorders (e.g., schizophrenia, and other diagnoses that may influence compliance)
  • Drug or alcohol abuse
  • Continuous oral pharmacological treatment and other types of pharmacological treatment that may influence the study
  • Present or recent usage of other probiotic agents
  • Other conditions which the investigator considers could negatively affect the outcome of the study or study compliance

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

81 participants in 3 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Four capsules containing rice flour will be given to the placebo group daily.
Treatment:
Dietary Supplement: LB001
Single dose
Experimental group
Description:
Two capsules of probiotics and two capsules of placebo daily. Probiotic capsules contains strains of pediococcus (Bacterial family of Lactobacillaceae) and saccharomycetes (kingdom of Fungi and the division Ascomycota) with a concentration of 13 millions cfu/g. Other ingredients (including stabilization) include rice bran, vegetable L-Cystein, magnesium salts from vegetable fatty acids. The capsule shell is made of vegetable HydroxyPropylMetylCellulosa (HPMC). Each capsule has a weight of 0.4 gram. The placebo is made of rice flour.
Treatment:
Dietary Supplement: LB001
Double dose
Experimental group
Description:
Four capsules of probiotics daily. Probiotic capsules contains strains of pediococcus (Bacterial family of Lactobacillaceae) and saccharomycetes (kingdom of Fungi and the division Ascomycota) with a concentration of 13 millions cfu/g. Other ingredients (including stabilization) include rice bran, vegetable L-Cystein, magnesium salts from vegetable fatty acids. The capsule shell is made of vegetable HydroxyPropylMetylCellulosa (HPMC). Each capsule has a weight of 0.4 gram.
Treatment:
Dietary Supplement: LB001

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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