Intestinal constipation
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Men and women aged 19-70 who have low evacuation frequency (2-4 days \ week) and general abdominal discomfort
Exclusion criteria
Exclusion criteria: Volunteers who have diagnosed diseases in the GIT or complications of surgeries resulting from these diseases; presence of hepatic or renal dysfunction; those who have used antibiotics in the last four weeks. Have used in the last four weeks drugs or vitamins or minerals or herbal foods or supplements to reduce digestive symptoms. Those who consumed food containing probiotics and prebiotics before and during the intervention. Volunteers consuming nutraceutical foods with anti-inflammatory activity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| If probiotics improve intestinal transit time, evacuation frequency, stool consistencies, and intestinal microbiota composition by increasing the concentration of SCFA in individuals with intestinal constipation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1- Evaluate which type of vehicle provides the best results: sachet or capsule ;2- If the number of strains present in the product influences the response to probiotics ;3- If dose of strains present in the product influences the response to probiotics | — |
Countries
Brazil
Contacts
Universidade de Brasília