About this trial
The purpose of this study is to assess the drug absorption of oral antibiotics in patients with short bowel syndrome.
Eligibility criteria
Qualifiers
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 Hospital of Nancy
Affiliated to a social security system
Disqualifiers
Patient at risk of worsening their oral absorption abilities during study
Patient requiring dialysis
Women of childbearing age without efficient birth control
Allergy to any of the drugs tested
Trial design
Treatments tested in this trial
- Amoxicillin
- Levofloxacin
- Ofloxacin
- Sulfamethoxazole trimethoprim
Treatment groups
Sponsors and collaborators
Central Hospital, Nancy, France
Lead sponsor
Société Francophone Nutrition Clinique et Métabolisme
Collaborator
FIlière des Maladies rares Abdomino-THOraciques
Collaborator
Fresenius Kabi
Collaborator