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Effect of Probiotics on intestinal health in adults and healthy adults

Effect of Probiotics on intestinal health in adults and healthy adults: Influence of the type of cepa, dose and method of administration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2qvnq9
Enrollment
Unknown
Registered
2019-06-04
Start date
2017-11-13
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intestinal constipation

Interventions

The selected individuals will be randomized into the following 08 groups: - Placebo 1 that will receive maltodextrin in a sachet
- Placebo 2 that will receive maltodextrin in capsule
-Lacto sachet that will receive 4 x 108 CFU of Lactobacillus acidophilus (SD 5221) in sachet
- Lacto capsule that will receive 4 x 108 CFU of Lactobacillus acidophilus (SD 5221) in capsules
- Lacto sachet 2 that will receive 4 x 108 CFU of Lactobacillus acidophilus + 5 g of lactitol (additive that will give a better flavor to the product)
- Flora 5 sachet that will receive a sachet containing a mix of probiotics consisting of 109 CFU of Lactobacillus acidophilus (SD 5221), Lactobacillus casei (Lc-11), Lactococcus lactis (Ll-23), Bifido
- Flora 5 capsule that will receive a capsule containing a mix of probiotics consisting of 109 CFU of Lactobacillus acidophilus (SD 5221), Lactobacillus casei (Lc-11), Lactococcus lactis (Ll-23), Bifi
- Flora 20 that will receive a capsule containing a mix of probiotics consisting of 4 x 109 CFU of Lactobacillus acidophilus (SD 5221), Lactobacillus casei (Lc-11), Lactococcus lactis (Ll-23), Bifidob
Dietary supplement
G07.203.300.456.500

Sponsors

Patrícia Borges Botelho
Lead Sponsor
Cifarma Científica Farmacêutica LTDA
Collaborator

Eligibility

Age
19 Years to 70 Years

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

MeasureTime 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

MeasureTime 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

Public ContactPatrícia Botelho

Universidade de Brasília

patriciaborges.nutri@gmail.com+55 -061 981806716

Outcome results

None listed

Source: REBEC (via WHO ICTRP)