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Clinical Trial Summary

Delivery of FMT by upper route, including gastroscopy, nasogastric/ nasojejunal tube, and lower route, including retention enema, sigmoidoscopy, or colonoscopy have all been utilized successfully. Endoscopic delivery requires significant health care utilization and associated cost. Therefore, it is extremely desirable if FMT can be infused by a non invasive modality, which would significantly reduce patient discomfort, procedure related risks and health care costs, while offering similar efficacy to colonoscopic delivery in the range of 90%.


Clinical Trial Description

Patients with minimum 3 episodes of Clostridium difficile within 6 months are randomized 1:1 to received FMT by either colonoscopy or capsules. Pts are assessed at 1 week, 2 weeks, 1 mon, 3 mon, 6 mon and 1 year post FMT. Stool, urine and blood samples are collected. Medical cost for previous treatment is collected as well at pt perspective and QoL. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02254811
Study type Interventional
Source University of Alberta
Contact
Status Completed
Phase Phase 2/Phase 3
Start date September 18, 2014
Completion date September 13, 2017

See also
  Status Clinical Trial Phase
Completed NCT02299570 - Microbiota Restoration Therapy for Recurrent Clostridium Difficile Infection Phase 2