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NCT05213910

Study of a Management Strategy of Functional Bowel Disordes Related to Irritable Bowel Syndrome (IBS) With a Mixture of 8 Microbiotic Strains

Completed NA Last updated 6 April 2022
What this trial tests

NA trial testing Lactichoc in Irritable Bowel Syndrome in 189 participants. Completed in 15 November 2021.

Timeline
4 September 2018
Primary endpoint
15 November 2021
15 November 2021

Quick facts

Lead sponsorPiLeJe
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment189
Start date4 September 2018
Primary completion15 November 2021
Estimated completion15 November 2021
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

PiLeJe — full company profile →

Who can join

Adults 18 to 75, any sex, with Irritable Bowel Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to determine the impact of a 10-day treatment with Lactichoc® on irritable bowel syndrome.

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Irritable Bowel Syndrome

Currently open trials in the same condition.

Other PiLeJe trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05213910.

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