Informations générales (source: ClinicalTrials.gov)
Study of Gut Microbiota in Crohn's Disease Patients Suffering From Spondylarthritis (FLORACROHN)
Interventional
N/A
Central Hospital, Nancy, France (Voir sur ClinicalTrials)
mars 2017
décembre 2020
29 juin 2024
The FLORACROHN project aims to compare gut microbiota of patients suffering from Crohn's
disease (CD) associated or not to spondylarthritis (SpA).
3 groups of patients will be analyzed: patients suffering from CD alone, patients
suffering from SpA alone, patients suffering from CD and SpA.
Fecal microbiota will be determined by 16SRNA gene sequencing.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| CHRU de Nancy - 54511 - Vandoeuvre les Nancy - France | Laurent PEYRIN-BIROULET, MD, PHD | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Patients with Crohn's disease and axial spondyloarthritis according to the criteria
below.
- Patients with Crohn's disease (CT patients) diagnosed according to clinical,
biological, radiological, endoscopic and / or histological criteria for 3
months. With diagnosis of spondyloarthritis exclusion on modified ASAS and / or
New York criteria.
- Patients with axial spondyloarthritis (SpA patients) diagnosed according to the
modified ASAS and / or New York criteria with exclusion diagnosis of Crohn's
disease.
- Patient with the capacity to give free and informed consent.
- Patients with Crohn's disease and axial spondyloarthritis according to the criteria
below.
- Patients with Crohn's disease (CT patients) diagnosed according to clinical,
biological, radiological, endoscopic and / or histological criteria for 3
months. With diagnosis of spondyloarthritis exclusion on modified ASAS and / or
New York criteria.
- Patients with axial spondyloarthritis (SpA patients) diagnosed according to the
modified ASAS and / or New York criteria with exclusion diagnosis of Crohn's
disease.
- Patient with the capacity to give free and informed consent.
Antecedent of colonic resection
- Antibiotic or colonic colonoscopy preparation in the 8 weeks prior to stool
collection (against temporary indication = collection possible before colic
preparation or on the first saddle after the start of the colic preparation).
- Ostomy at time of collection
- BMI> 30
- extreme diet
- unbalanced diabetes
- Patient under guardianship, under curatorship or under safeguard of justice