Absorption of Antibiotics With High Oral Bioavailability in Short-bowel Syndrome

Recruiting Phase 1 Interventional Study
Short Bowel Syndrome Infection, Bacterial
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
10 (estimated)
Sponsor
Central Hospital, Nancy, France · Other
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About This Trial

The purpose of this study is to assess the drug absorption of oral antibiotics in patients with short bowel syndrome.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Short bowel syndrome * Treated for a documented infection with antibiogram by amoxicillin (+/- clavulanic acid)or ofloxacin or levofloxacin or sulfamethoxazole/trimethoprim * Hospitalized in the Nutritional Assistant Unit or the Infectiology Unit of the Regional University Hos…
Contacts

Niasha MICHOT, MD

+33383155108

n.michot@chru-nancy.fr

CONTACT

Elise Pape

e.pape@chru-nancy.fr

CONTACT