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🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2026-07-08)

The Effect of Humiome® Post LB on Gut COMFort in healthY Adult Volunteers

🟢 Recruiting Protocol / Phase N/A 🥗 Dietary & Nutritional Intervention Sponsor: dsm-firmenich Switzerland AG

🩺 Protocol Summary

The goal of this double-blind, randomized placebo-controlled study is to evaluate the effect of an 8-week supplementation of Humiome ® Post LB (170 mg) on bowel movements in healthy adult volunteers compared to Placebo adjusted on baseline. The main question\[s\] it aims to answer \[is/are\]: Does Humiome ® Post LB improve bowel movements with self-reported GI issues? Participants will be provided Humiome ® Post LB (170 mg) for 8 weeks and asked to complete a study diary, questionnaires, and stool samples.

Primary Research Facility: KGK Science Inc. (London, Ontario)

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📍 Primary Site Map

Site: KGK Science Inc. — London, Ontario

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🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT06937814 • Last Synced: 2026-07-08
View on ClinicalTrials.gov ↗
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