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Changes in Microbiota and Quality of Life in IBS - Trial NCT05266287

Access comprehensive clinical trial information for NCT05266287 through Pure Global AI's free database. This phase not specified trial is sponsored by National University of Natural Medicine and is currently Not yet recruiting. The study focuses on IBS - Irritable Bowel Syndrome. Target enrollment is 50 participants.

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NCT05266287
Not yet recruiting
dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT05266287
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Changes in Microbiota and Quality of Life in IBS
Evaluating Changes in Microbiota Composition and Quality of Life in Irritable Bowel Syndrome: A Randomized, Controlled Trial

Study Focus

a supplement containing 2'-fucosyllactose (2'-FL)

Interventional

dietary supplement

Sponsor & Location

National University of Natural Medicine

Timeline & Enrollment

N/A

Mar 01, 2022

Dec 31, 2022

50 participants

Primary Outcome

F. Prausnitzii abundance

Summary

The primary research question to be addressed is: Does a 2'-FL-containing dietary supplement
 impact stool microbiota composition in adults with IBS? The primary measure for determining
 potential impacts of the 2'-FL-containing dietary supplement on stool microbiota composition
 is stool abundance of Faecalibacterium prausnitzii, a commensal intestinal bacteria.
 Additional measures related to determining potential impacts of the 2'-FL-containing dietary
 supplement on gut microbiota composition are stool levels of additional commensal intestinal
 bacteria and measures of intestinal microbial diversity.

ICD-10 Classifications

Irritable bowel syndrome with predominant constipation [IBS-C]
Irritable bowel syndrome
Irritable bowel syndrome with predominant diarrhoea [IBS-D]
Irritable bowel syndrome with mixed bowel habits [IBS-M]
Other and unspecified irritable bowel syndrome

Data Source

ClinicalTrials.gov

NCT05266287

Non-Device Trial