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Clinical Trial Summary

Multicentre prospective human experimental study to determine the effect of chyme reinfusion in patients with a double enterostomy on plasma levels of Fibroblast Growth Factor (FGF19)


Clinical Trial Description

Patients supported by chyme reinfusion will be followed for 3 days pre chyme reinfusion and for 7 weeks during chyme reinfusion. Three days prior chyme reinfusion, baseline characteristics will be determined, an ileal biopsy, blood, chyme and urine will be collected. Furthermore, blood, chyme, faeces and urine will be collected at the first day of chime reinfusion. These materials will be collected again at week 1, 3, 5 and 7 weeks after initiation of chyme reinfusion. A second ileal biopsy will be performed at week 3. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02990195
Study type Interventional
Source Rennes University Hospital
Contact
Status Completed
Phase Phase 2
Start date December 1, 2016
Completion date July 2, 2018