Interventions to Decrease the Impact of Post-OPerative Ileus After Liver Transplant or Resection Surgery

Ileus Clinical Trial

Official title: Interventions to Decrease the Impact of Post-Operative Ileus After Liver Transplant or Resection Surgery

Status Completed

Clinical Trial Summary

This is a randomized controlled trial to assess ways to address post-operative ileus (POI) in adult patients on the liver transplant service undergoing either liver transplant or resection surgery. Patient who speak and understand English will be randomized into one of three groups including a.)control group receiving standard therapy for post-operative ileus, b.)group receiving standard therapy and acupressure bracelets, and c.)group receiving standard therapy and sugar free gum four times daily.

Clinical Trial Description

Any patient undergoing liver transplant or resection surgery will be asked to participate in the study and assigned to a control or investigational group. Pertinent information will be collected from the medical record including gender, age in years, diagnosis, type of surgery, length of stay, medications used for pain or nausea, and first bowel movement. The subjects will also be asked to keep a journal of their bowel habits, signs and symptoms of gastrointestinal distress/post-operative ileus, use of medications, first bowel movement, satisfaction with bowel management and any additional comments.

Aims of the study are to determine the effectiveness of the three arms of this trial for the resolution of POI as noted by first post-operative bowel movement; to determine if there is a difference in the length of stay based on the interventions; and to determine if there is a difference in patient satisfaction based on the intervention. ;

Related Conditions & MeSH terms

• Ileus

• NCT number: NCT01156129
• Study type: Interventional
• Source: University of Nebraska
• Status: Completed
• Phase: Phase 1
• Start date: September 1, 2010
• Completion date: December 1, 2012