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NCT05482464

Effect of Daily Consumption of Glycomacropeptide on Gut Microbiome and Blood Functional Proteome of Subjects With Irritable Bowel Syndrome

Completed NA Last updated 4 April 2025
What this trial tests

NA trial testing Casein glycomacropeptide (CGMP) in Inflammatory Bowel Syndrome in 15 participants. Completed in 1 September 2024.

Timeline
1 January 2022
Primary endpoint
1 September 2024
1 September 2024

Quick facts

Lead sponsorOregon State University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment15
Start date1 January 2022
Primary completion1 September 2024
Estimated completion1 September 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Oregon State University

Who can join

Adults 18 to 30, any sex, with Inflammatory Bowel Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study investigates the use of glycomacropeptide (GMP) as a means to manipulate the gut microbiome, metabolome and protein profile of subjects with irritable bowel syndrome (IBS).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Evaluating the Potential of Casein Glycomacropeptide in Adult Irritable Bowel Syndrome Management: A Pilot Study.
    Qu Y, Park SH, Dallas DC. · · 2023 · cited 3× · PMID 37836457 · DOI 10.3390/nu15194174

Verify or expand the search:

Other trials of Casein glycomacropeptide (CGMP)

Trials testing the same drug.

Other recruiting trials for Inflammatory Bowel Syndrome

Currently open trials in the same condition.

Other Oregon State University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05482464.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing