Last reviewed · How we verify

NCT03274648

Dietary Interventions and Butyrate Production in Behçet's Patients

Completed NA Last updated 28 January 2020
What this trial tests

NA trial testing Oral butyrate in Behcet Syndrome in 17 participants. Completed in 5 July 2019.

Timeline
27 September 2017
Primary endpoint
1 May 2019
5 July 2019

Quick facts

Lead sponsorAzienda Ospedaliero-Universitaria Careggi
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment17
Start date27 September 2017
Primary completion1 May 2019
Estimated completion5 July 2019
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Azienda Ospedaliero-Universitaria Careggi — full company profile →

Who can join

Adults 18 to 70, any sex, with Behcet Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A dietary intervention trial will be performed on patients affected by Behçet's syndrome. Three different diets will be compared, analyzing their effects on the gut microbiota composition, on endogenous butyrate production and on the general symptoms in Behçet's patients.

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 recruiting trials for Behcet Syndrome

Currently open trials in the same condition.

Other Azienda Ospedaliero-Universitaria Careggi 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/NCT03274648.

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