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Clinical Trial Summary

The aim of this study is to compare postoperative ileus between stimulated and unstimulated patients prior to ileostomy closure.


Clinical Trial Description

Stimulation was performed ten days prior to the intervention, through the efferent limb of the ileostomy with 500 cc of a thickening substance (saline and nutritional thickener) ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01881594
Study type Interventional
Source Hospital Universitario Virgen de la Arrixaca
Contact
Status Completed
Phase Phase 3
Start date January 2012

See also
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