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CompletedNCT04596605

Gastrointestinal Tolerance Assessment of T2309

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
55 (actual)
Sponsor
Laboratoires Thea · Industry
Sex
All
Age
50 Years
Healthy volunteers
Accepted

Summary

Gastrointestinal Tolerance assessment of T2309 compared to a food supplement in 50 subjects.

Conditions

Interventions

TypeNameDescription
OTHERT2309Food for Special Medical Purpose / 4 capsules daily for 12 weeks
DIETARY_SUPPLEMENTNutrof Total2 capsules daily for 12 weeks

Timeline

Start date
2020-07-15
Primary completion
2021-03-04
Completion
2021-03-04
First posted
2020-10-22
Last updated
2021-07-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04596605. Inclusion in this directory is not an endorsement.

Gastrointestinal Tolerance Assessment of T2309 (NCT04596605) · Clinical Trials Directory