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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04280731
Other study ID # FermCH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 7, 2020
Est. completion date June 20, 2020

Study information

Verified date October 2020
Source Lund University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The demand for alternatives to dairy products has increased in recent years and a lot of proposals for vegetable milk and yogurt products have taken place in the market. Quinoa is a plant from South America that has growth in popularity in recent years as many sought out nutritious and healthier eating, the herb is known for its high nutritional value. It is complete protein source containing all the essential amino acids. If this herb were fermented with probiotic bacteria, there is a potential for a product that is lactose free, gluten free and cholesterol free.

The probiotic potential of quinoa milk, fermented with food associated lactic acid bacteria will be investigated. This includes a study that examines how daily consumption of this vegetable drink changes the composition of the oral and intestinal flora. Therefore, healthy people are now seeking to participate in the study, which will be for just over 2 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 20, 2020
Est. primary completion date June 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Above 18 years and healthy volunteers

Exclusion Criteria:

- Participants that have any kind of diseases, such as colon inflammation

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
fermented quinoa
Quinoa drink fermented with lactic acid bacteria isolated from food

Locations

Country Name City State
Sweden Kemicentrum Lund Skåne

Sponsors (2)

Lead Sponsor Collaborator
Lund University Swedish International Development Cooperation Agency (SIDA)

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survivability of the lactic acid bacteria If the bacteria can be isolated in a adequate amount by cultivation on MRS broth and rogosa agar 2 weeks
Secondary Changes in the human microbiota Changes in the saliva and stool samples by analyzes with Terminal Restriction Fragment Length polymorphism 2 weeks
Secondary Changes in the human microbiota Changes in the saliva and stool samples by quantitative polymorphic chain reaction 2 weeks
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