Fecal Microbiota Alterations in Steroid Refractory Active Colitis Ulcerosa
NCT ID: NCT03460847
Last Updated: 2021-09-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
114 participants
OBSERVATIONAL
2018-03-01
2021-03-01
Brief Summary
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Detailed Description
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The investigators therefore plan to investigate the intestinal microbiota in UC patients before and 4 weeks after a systemic corticosteroid therapy and correlate potential alterations of the microbiota to the therapeutic response. Other factors like concomitant UC treatment, disease severity, disease extent and environmental factors will also be correlated to changes in the microbiota.
In the subgroup of patients not responding to steroids and requiring a rescue therapy with infliximab or a calcineurin Inhibitor, the predictive value of microbiota alterations will also be investigated.
If certain bacterial taxa can predict a steroid refractory and an unfavorable disease course, the results of this study will help in identifying possible microbiota based biomarkers for an individualized treatment approach in UC patients in the future.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Steroids
Patients with active colitis ulcerosa who need steroids because of their disease course. 1mg/kg bodyweight for one week, followed by a tapping periode.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patient scheduled for steroid therapy with systemic steroids (prednisolone or methylprednisolone) at standard dosing and patients who started steroid therapy not longer than 48 hours prior to the study inclusion.
* Written informed consent
* Established or suspected diagnosis of ulcerative colitis or indeterminate colitis
Exclusion Criteria
* Bacterial intestinal infections (C. difficile, Salmonella, EHEC, Campylobacter, Shigella, Yersinia), parasitic or viral infection causing acute infectious diarrhea at baseline.
* Diagnosis of Crohn´s disease
* Planned initiation or discontinuation of probiotic therapy between baseline and follow up visit
18 Years
ALL
No
Sponsors
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Medical University of Graz
OTHER
Responsible Party
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Principal Investigators
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Christoph Hoegenauer, Prof.
Role: PRINCIPAL_INVESTIGATOR
Medical University of Graz
Locations
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LKH Graz
Graz, Styria, Austria
Countries
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Other Identifiers
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29-316 ex 16/17
Identifier Type: -
Identifier Source: org_study_id
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