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NCT06945302

The Effect of Inulin Supplementation in Individuals With IBS-C

Completed NA Last updated 25 April 2025
What this trial tests

NA trial testing Intervention Group in Inulin in 34 participants. Completed in 1 April 2023.

Timeline
3 November 2021
Primary endpoint
3 January 2022
1 April 2023

Quick facts

Lead sponsorMardin Artuklu University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment34
Start date3 November 2021
Primary completion3 January 2022
Estimated completion1 April 2023
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Mardin Artuklu University

Who can join

Adults 19 to 65, any sex, with Inulin or IBS (Irritable Bowel Syndrome). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Background: This study aimed to evaluate the effects of inulin supplementation on nutritional intake, anthropometric parameters, and bowel symptoms in individuals diagnosed with IBS-C. Method: This was a randomised, single-blind, placebo-controlled clinical trial. Participants were randomly allocated into intervention (inulin) and control (placebo) groups for 8 weeks. Assessments included dietary intake, anthropometric measurements, and IBS symptoms.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Intervention Group

Trials testing the same drug.

Other Mardin Artuklu University trials

Trials by the same sponsor.

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Data sources for this page

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