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Impact of Butyricicoccus Pullicaecorum in Healthy Subjects

Healthy Clinical Trial

Official title:
A Placebo-controlled Cross-over Randomized Study to Investigate the Impact of Butyricicoccus Pullicaecorum in Healthy Human Volunteers

Clinical Trial Summary

During this project the safety, tolerability and effect on gut microbiota of oral administration of Butyricicoccus pullicaecorum was investigated in healthy human volunteers by a placebo-controlled cross-over randomized study.

Clinical Trial Description

Intervention periods were 4 weeks, with daily intake of 1 capsule. Wash-out periods were 3 weeks. ;

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02477033
Study type Interventional
Source Katholieke Universiteit Leuven
Contact
Status Completed
Phase Phase 1
Start date February 2014
Completion date February 2015
View Details
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