Clinical trial
A Randomized, Cross-over, Placebo-Controlled, Double-Blind Clinical Trial on the Efficacy and Safety of Oral Administration of Postibiotic by FOS Fermentation From Lactobacillus Paracasei in the Treatment of Irritable Bowel Syndrome.
NCT06423001 is registered in ClinicalTrials.gov with Istituto Clinico Humanitas as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized, Cross-over, Placebo-Controlled, Double-Blind Clinical Trial on the Efficacy and Safety of Oral Administration of Postibiotic by FOS Fermentation From Lactobacillus Paracasei in the Treatment of Irritable Bowel Syndrome.
- Lead sponsor
- Istituto Clinico Humanitas
- Phase
- Not applicable
- Overall status
- Unknown status
- Start date
- June 15, 2024
- Completion date
- May 15, 2026
- Enrollment
- 36 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
ibs - irritable bowel syndrome