Early Feeding Following Percutaneous Gastrostomy Tube Placement



Status:Recruiting
Healthy:No
Age Range:18 - 80
Updated:12/29/2018
Start Date:October 30, 2017
End Date:November 2019
Contact:Lucy Smigiel
Email:lucy.smigiel@ucdenver.edu
Phone:720-848-6610

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This study plans to learn more about the safety of early feeding following placement of a
feeding tube. Doctors in other specialties feed patients 4 hours after patients receive a
feeding tube. However, Interventional Radiologists typically wait to feed patients for 24
hours following feeding tube placement. The investigator would like to demonstrate that
feeding after 4 hours does not increase complications and can actually reduce the burden to
patients who receive a feeding tube.


Inclusion Criteria:

- Patients between the ages of 18-80 years

- Outpatients receiving a gastrostomy tube at University of Colorado that do not require
post-pyloric feeding

- Patients that have no contraindication for intragastric feeding immediately following
tube placement

- INR (international normalized ratio) <1.5

- Platelet count > 50,000/µL

- WBC (white blood cell count) 4.0-11.1 x 109/L

Exclusion Criteria:

- Patients < 18 years or > 80 years of age

- Patients admitted to the hospital at the time of screening (i.e., inpatients)

- Women who are pregnant (confirmed by urine pregnancy screen)

- Patients requiring post-pyloric feeding

- Patients receiving venting gastrostomy tubes

- Patients receiving primary Gastro-Jejunal (GJ) Tube tube placement

- Patients with an interposed bowel on CT after stomach insufflation

- INR > 1.5

- Platelet count < 50,000/µL

- WBC > 11.1 x 109/L

- Known active infection

- Need for post-gastric feeding

- History of gastric bypass surgery or Roux-En-Y

- Mechanical obstruction of the GI tract

- Active peritonitis

- Known hemodynamic instability as demonstrated by tachycardia, hypotension, labile
blood pressure or altered mental status.

- Bowel ischemia

- Ascites

- Recent Gastro-Intestinal (GI) bleeding (within 2 weeks)

- Respiratory compromise as demonstrated by hypercarbia (CO2>45mmHg) or hypoxia (O2<90%)

- Unable to provide informed consent
We found this trial at
1
site
Aurora, Colorado 80045
Principal Investigator: Thor Johnson, MD, PhD
Phone: 720-848-6610
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mi
from
Aurora, CO
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