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NCT05416151

Effect of B.Lactis Consumption on Gastro-Intestinal (GI) Symptoms in Healthy Women Reporting Minor GI Symptoms

Completed NA Last updated 9 August 2024
What this trial tests

NA trial testing Freeze-dried biotic in Gastro-intestinal Symptoms in Healthy Subjects in 486 participants. Completed in 18 April 2024.

Timeline
24 May 2022
Primary endpoint
15 December 2023
18 April 2024

Quick facts

Lead sponsorDanone Global Research & Innovation Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposesupportive care
Enrollment486
Start date24 May 2022
Primary completion15 December 2023
Estimated completion18 April 2024
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Danone Global Research & Innovation Center — full company profile →

Who can join

Adults 18 to 60, female only, with Gastro-intestinal Symptoms in Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the effect of a 28-day B.lactis consumption twice daily on Gastro-Intestinal (GI) symptoms in healthy women reporting minor GI symptoms.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Danone Global Research & Innovation Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05416151.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing