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Identification of Fecal Microbiota Biomarkers of Spondyloarthritis in Patients Suffering From Crohn's Disease.

Study acronym: MICROSPA
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary completion pushed from Nov 4, 2026 to Nov 4, 2027
    • Study completion pushed from Dec 16, 2026 to Dec 16, 2027
    v7
  2. Re-verified, no change to tracked fieldsv6
  3. Primary completion date: Nov 4, 2025 to Nov 4, 2026
    • Study completion date: Dec 16, 2025 to Dec 16, 2026
    v5
  4. Primary completion date: Nov 4, 2024 to Nov 4, 2025
    • Study completion date: Dec 16, 2024 to Dec 16, 2025
    v4
  5. Study sites: 1 to 2v3
  6. Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Jul 2020 to Nov 4, 2024
    • Start date changed from estimate of Jul 2019 to Nov 16, 2021
    • Study completion date: Jul 2021 to Dec 16, 2024
    v2
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The MICROSPA project aims to compare gut microbiota, serum cytokines, and PBMC 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. One group of healthy controls will be analysed as a comparator. Fecal microbiota will be determined by bacteriome, virome and fungome NGS sequencing
Trial Details
NCT Number NCT03983473
Lead Sponsor Central Hospital, Nancy, France
Collaborators: Centre Hospitalier Régional Metz-Thionville, University Hospital, Strasbourg, France, Saint Antoine University Hospital
Conditions
(from sponsor)		 Crohn Disease, Spondyloarthritis
Related terms Crohn Disease, Spondylarthritis
Enrollment 240 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov