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Clinical Trial Summary

The study will characterize the biology of FMT in the context of IBS prior to wider clinical application of the method. Given the ethical concerns of unknown and long-term adverse effects of FMT therapy, the study will include patients only with moderate to severe symptoms. IBS is a heterogenous disorder and it is important to characterize the patients, and study as homogeneous patient populations as possible. Therefore the study will only include post-infectious IBS patients after the Giardia outbreak.


Clinical Trial Description

Primary aims:

Detailed characterisation of donor and recipient microbial community composition (by means of 16S rRNA profiling) and determination of the kinetics of changes following FMT

Secondary aims:

- Determination of interactions of importance to persisting recipient gut microbiota.

- Evaluate safety of FMT in an IBS population

- To evaluate the efficacy of FMT in relieving symptoms in selected patients with IBS in an open pilot trial in order to have the possibility to calculate number of patients needed when planning future controlled studies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03333291
Study type Interventional
Source Haukeland University Hospital
Contact
Status Completed
Phase N/A
Start date October 1, 2016
Completion date June 30, 2017

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