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Status unknownNCT05676229Updated Feb 21, 2023

Probiotic Blend in Reducing Anthropometric Measurements in Obese Adults

A Phase 2 interventional study of Probiotic blend and Placebo in Obesity, Obesity; Endocrine and Overweight and Obesity, sponsored by Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude. Status unknown at 1 site in Brazil. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-02-21.

Sponsored by Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude · Phase 2, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Feb 2023), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

It is already known that dysbiosis, that is, qualitative and quantitative changes in the composition of the intestinal microbiota, can be associated with the development of a series of intestinal and extra-intestinal disorders. Dysbiosis is reported in irritable bowel syndrome, inflammatory bowel disease, colorectal cancer, allergic diseases, non-alcoholic steatohepatitis, arteriosclerotic diseases, neurological diseases and metabolic syndromes, mainly diabetes and obesity. Among the many factors that play a key role in obesity, a number of studies show the intestinal microbiota as an important contributor. Many studies carried out with probiotics have shown that their administration can be effective in the prevention and treatment of obesity. Furthermore, it is found that benefits for body weight, abdominal adiposity, anthropometric measurements and body composition are often associated with favorable metabolic effects.

Read the detailed description

Obesity is defined as excessive accumulation of body fat, caused by an energy imbalance. Approximately 13% of the world's adult population is obese, and in Brazil 19.8% of adults are obese. This disease is a risk factor for the development of other non-communicable chronic diseases (NCDs), such as: type 2 diabetes mellitus (DM2), dyslipidemia, cardiovascular diseases, musculoskeletal disorders and some types of cancer. It is a complex and multifactorial disease, which is why it is considered difficult to control and a cause for global concern. Among the causes of the disease, genetic, environmental and psychological factors can be mentioned, in addition to the interference of the intestinal microbiota, among others.

The interaction of the intestinal microbiota with the host has been studied through metabolomics, in order to understand the influence that the microbiota can exert on the functioning of the host organism. The study of the profile of low molecular weight metabolites of biological fluids such as serum/plasma and urine aims to understand the metabolic changes that occur in individuals with obesity, encompassing the understanding of the mechanisms of the disease.

Studies have shown differences in the metabolic profile of obese individuals compared to eutrophic individuals, with a positive correlation between body mass index (BMI) and increased concentrations of chain amino acids (BCAA) and glutamate. The gut microbiota appears to play a crucial role in host metabolism, being a pathway through which it leads to changes associated with obesity.

In this context, the intestinal microbiota can be modulated by prebiotics, probiotics and symbiotics, promoting changes in its composition, resulting in the regeneration of the intestinal barrier and, with that, ceasing metabolic endotoxemia and low-grade inflammation.

In addition, they have effects on the modulation of the immune system, regulating the production of pro and anti-inflammatory cytokines, reducing IR. Through these mechanisms, probiotics and symbiotics alter the microbiota profile of individuals leading to loss of body weight and metabolic parameters associated with obesity.

Several studies have shown beneficial effects of using probiotics on body weight, glycemic control, improvement in lipid profile and blood pressure (BP). However, there are controversies about which are the best strains for this purpose. There are five systematic reviews currently published with or without meta-analysis that address the effect of using different probiotics on body weight. Among the strains associated with weight loss and/or adiposity, L. plantarum associated with L. rhamnosus and hypocaloric diet stand out; L. plantarum with L. curvatus; L. gasseri; L. amylovorus; L. acidophilus and L. casei associated with phenolic compounds; or Lactobacillus mix.

02

Conditions studied

  • Obesity
  • Obesity; Endocrine
  • Overweight and Obesity
  • Overweight, Obesity and Other Hyperalimentation

Keywords

  • obesity
  • probiotic
  • supplement
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's planned enrollment of 108 is above the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude is the lead sponsor of 13 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Provision of Free and Informed Consent in writing, signed and dated;
  • Age according to the indicated population (18-65 years old)
  • both genders;
  • Body mass index (BMI) of 25 - 35 Kg/m2.

Exclusion criteria

Exclusion Criteria:

  • Pregnant and lactating women
  • Individuals with a history of daily consumption of probiotics, fermented milk and/or yogurt; subjects known to have demonstrated a prior reaction, including anaphylaxis, to any substance in the composition of the study product;
  • Individuals with concomitant participation in another clinical trial;
  • History of autoimmune, cardiovascular, thyroid, or chronic liver disease;
  • Making use of medication capable of affecting weight change, antidiabetic medication, hypolipidemic agents;
  • Individuals who have undergone weight loss surgery,
  • Weight change greater than 5% in the last three months.
05

Study design

Phase
Phase 2
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
108 participants (estimated)

Study arms

  • Placebo comparator
    Placebo

    Volunteers supplemented with maltodextrin

    Dietary Supplement: Placebo

  • Active comparator
    Probiotic Blend

    Lactobacillus gasseri CCT 7850 and Bifidobacterium lactis CCT 7858 - Final concentration: 1 x 10e10 UFC/ day

    Dietary Supplement: Probiotic blend

Interventions

  • Dietary supplementProbiotic blend

    Lactobacillus gasseri CCT 7850 and Bifidobacterium lactis CCT 7858

  • Dietary supplementPlacebo

    Maltodextrin only (vehicle)

06

What researchers measure

Primary outcomes

  1. Body fat composition by Bioelectrical impedance analysis

    By Bioelectrical impedance analysis (BIA). This is a method for estimating body composition, in particular body fat and muscle mass, where a weak electric current flows through the body and the voltage is measured in order to calculate impedance (resistance) of the body.

    Time frame: three months

Secondary outcomes

  1. Total cholesterol by blood analyses

    biochemical analyses before and after inclusion: Total cholesterol to be carried out in a reference laboratory. Total cholesterol will be measured in mg/dL

    Time frame: three months

  2. quality of life questionnaire score

    quality of life and improvement of gastrointestinal symptoms by SF-36 scale (It comprises 36 questions that cover eight domains of health)

    Time frame: three months

  3. Gastrointestinal Symptom Rating Scale (GSRS) questionnaire score

    GSRS scale: An interview-based rating scale consisting of 15 items for assessment of gastrointestinal symptoms

    Time frame: three months

  4. Weight

    weight will be measured in kilograms

    Time frame: three months

  5. height

    height will be measured in centimeters

    Time frame: three months

  6. HDL levels by blood analyses

    biochemical analyses before and after inclusion: HDL to be carried out in a reference laboratory. HDL will be measured in mg/dL

    Time frame: three months

  7. LDL levels by blood analyses

    biochemical analyses before and after inclusion: LDL to be carried out in a reference laboratory. LDL will be measured in mg/dL

    Time frame: three months

  8. triglycerides levels by blood analyses

    biochemical analyses before and after inclusion: triglycerides to be carried out in a reference laboratory. triglycerides will be measured in ml/dL

    Time frame: three months

  9. Glucose levels by blood analyses

    biochemical analyses before and after inclusion: glucose to be carried out in a reference laboratory. glucose will be measured in mg/dL

    Time frame: three months

07

Study locations

1 of 1 sites recruiting
  • Universidade do Extremo Sul Catarinense
    Criciúma, Santa Catarina 88806-000, Brazil
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05676229
Lead sponsor
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
Responsible party
Monique Michels (PhD, Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude) — Principal investigator
First posted
Jan 9, 2023
Start date
Jan 11, 2023
Primary completion
Feb 19, 2023
Completion
Dec 30, 2023 (estimated)
Last update
Feb 21, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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