Last reviewed · How we verify

NCT03824821: IBSQUtrition

Assessing Associations Between IBS Symptoms, Nutrition and QoL in IBS Patients Using a Questionnaire

Completed Last updated 31 January 2019
What this trial tests

trial testing No intervention in Irritable Bowel Syndrome in 2,076 participants. Completed in 31 May 2018.

Timeline
22 January 2018
Primary endpoint
31 May 2018
31 May 2018

Quick facts

Lead sponsorWageningen University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,076
Start date22 January 2018
Primary completion31 May 2018
Estimated completion31 May 2018
Sites1 location across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Wageningen University

Who can join

18 and older, any sex, with Irritable Bowel Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a cross-sectional observational study design that aimed to include 2000 IBS patients. We used several validated questionnaires, to assess IBS characteristics (such as subtype, severity), psychological features (QoL, anxiety and depression) and assess nutritional triggers. Subjects filled in the questionnaire online, and was spread across the Netherlands.

Publications & conference data

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

Verify or expand the search:

Other trials of No intervention

Trials testing the same drug.

Other recruiting trials for Irritable Bowel Syndrome

Currently open trials in the same condition.

Other Wageningen 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/NCT03824821.

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