Optimizing the Previs Device for Prediction of Postoperative Ileus



Status:Recruiting
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 100
Updated:3/16/2019
Start Date:April 24, 2018
End Date:December 2021
Contact:Debra OConnell Moore, MBA
Email:debra-oconnell-moore@uiowa.edu
Phone:319-356-1693

Use our guide to learn which trials are right for you!

The research proposed in this study will develop a noninvasive prototype device that will
capture intestinal sounds, process signals, and display predictive information in real-time
at the point-of-care using algorithms already developed at this institution.

Following major abdominal surgery, up to 30% of patients develop a poorly understood
condition known as ileus. When ileus occurs, the bowels shut down and patients often develop
abdominal dissension, nausea, vomiting, and even more serious complications. Because this
condition does not develop until many days after surgery has been completed, clinicians do
not know if they should begin allowing patients to eat or withhold nutrition until they show
signs of bowel function such as passing gas or having bowel movements. Clinicians have
different approaches but none are ideal: 1) feed all patients early and the ones that develop
an ileus will have their diets reverse, suction tube placed in their stomach, and hopefully
don't get develop more serious complications, or 2) don't feed patients until they pass gas
or have a bowel movement, which delays nutrition and prolongs hospital stays for the 70% of
patients who will not develop an ileus

Participants in this study will be asked to wear a 3-ounce device that adheres to the skin of
the abdominal wall for 10 days. They will also be asked to answer questions each day of their
hospital stay regarding how they have tolerated eating.

Inclusion Criteria:

Patients undergoing elective intestinal resection surgery by the colorectal surgery service
at UIHC.

Age 18 to 100.

Exclusion Criteria:

Allergies to any of the device components. Inability to have prototype device applied to
their abdominal wall due to a condition (ie:fistulas, stomas, drains, etc).
We found this trial at
1
site
101 Jessup Hall
Iowa City, Iowa 52242
(319) 335-3500
Phone: 319-356-1722
University of Iowa With just over 30,000 students, the University of Iowa is one of...
?
mi
from
Iowa City, IA
Click here to add this to my saved trials