Assessing Changes in the Gut Microbiome of Non-Gastrointestinal Disordered Subjects Before and After Oral Prebiotic Supplementation Using the SIMBA Capsule

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexMale
Age19-40
SponsorNimble Science Ltd.

About this trial

This is a randomized, double-blind, placebo-controlled, parallel-group clinical study. The primary objective is to assess the changes in the small intestinal (SI) metagenomic profile of healthy participants without any known gastrointestinal disorders from baseline to endpoint in response to the prebiotic intervention (FiberSmart). The study population are adults (n=30) who will ingest either the FiberSmart or a matched Placebo daily for 21 days. Both products will be referred to as the Investigational Product (IP) in the study procedures section. While prebiotics are widely used for gut health, their specific impact on the small intestinal ecosystem remains largely uncharacterized compared to the large intestine. Understanding their impact on the upper GI tract can lead to new insights into their mechanisms of action. Given the critical role of the small intestine in metabolism and immunity, the study utilizes the SIMBA capsule to measure novel changes in the small intestine along with traditional measurements from stool samples.

Eligibility criteria

Qualifiers

Aged 19-40 years old at the inclusion of the study, both female and male subjects.

Either a male or a non-pregnant, non-lactating female, at least 6 weeks postpartum prior to the Baseline Visit.

Willing to maintain their current lifestyle during the study.

Able to swallow a 25mm length and 9mm width sized capsule.

Disqualifiers

Use of any prescription medication within 14 days prior to the start of the study, which in the investigator's opinion, may interfere with the study results or pose a risk to the participant (excluding oral contraceptives).

Any current acute or chronic medical condition, which in the investigator's opinion, may interfere with the study results or pose a risk to the participant.

Known or suspected history of any gastrointestinal disease including, but not limited to, irritable bowel syndrome, celiac disease (treated or untreated), inflammatory bowel disease, persistent diarrhea, chronic constipation, gastrointestinal malignancy, or any condition known to affect gastrointestinal motility or absorption.

Less than 3 bowel movements a week

Trial design

Treatments tested in this trial

  • FiberSmart
  • Placebo

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators