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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05676229
Other study ID # 65117022.1.0000.0119
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date January 11, 2023
Est. completion date December 30, 2023

Study information

Verified date February 2023
Source Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Probiotic blend
Lactobacillus gasseri CCT 7850 and Bifidobacterium lactis CCT 7858
Placebo
Maltodextrin only (vehicle)

Locations

Country Name City State
Brazil Universidade do Extremo Sul Catarinense Criciúma Santa Catarina

Sponsors (1)

Lead Sponsor Collaborator
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. three months
Secondary 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 three months
Secondary 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) three months
Secondary Gastrointestinal Symptom Rating Scale (GSRS) questionnaire score GSRS scale: An interview-based rating scale consisting of 15 items for assessment of gastrointestinal symptoms three months
Secondary Weight weight will be measured in kilograms three months
Secondary height height will be measured in centimeters three months
Secondary 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 three months
Secondary 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 three months
Secondary 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 three months
Secondary 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 three months
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