Ileostomy; Complications Clinical Trial
The aim of this study is to compare postoperative ileus between stimulated and unstimulated patients prior to ileostomy closure.
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) ;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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