Impact of Carbon Dioxide Insufflation and Water Exchange on Post-Colonoscopy Outcomes

Completed · Not applicable

Conditions studied: Abdominal Pain

In brief

Room air insufflated during colonoscopy cannot be completely suctioned, is not easily absorbed and remains in the bowel for quite some time, resulting in prolonged bowel distension with the discomfort of bloating. Sufferers often experience a sensation of fullness and abdominal pressure, relieved only after expulsion of the residual gas, often accompanied by colic pain. This can be a lengthy process, and some patients continue to report pain as long as 24 hours after the procedure. Abdominal discomfort after colonoscopy is an adverse event commonly reported by patients, and definitely associated with the procedure. Published reports show that the use of carbon dioxide (CO2) insufflation significantly decreases bloating and pain up to 24 hours post-procedure. Preliminary results of the investigators' previous study about on-demand sedation colonoscopy in diagnostic patients showed that, compared with CO2 insufflation, the water exchange group (WE, infusion of water to distend the lumen during insertion; suction of infused water, residual air pockets an feces predominantly during insertion) achieved significantly lower real-time insertion pain scores. Moreover (insertion-withdrawal method) WE-CO2 had the lowest bloating scores just after the procedure and at discharge, comparable with those achieved by CO2-CO2. Compared with WE-CO2, the use of WE-air insufflation (AI) showed significantly higher bloating scores just after the procedure and at discharge; compared with CO2-CO2 differences were significant only at discharge. The investigators decided to conduct a prospective randomized controlled trial comparing WE-CO2, WE-AI and CO2-CO2. The investigators will test the hypothesis that patients examined by the combination of WE-CO2 will have significantly lower bloating scores at specific time points after colonoscopy than those examined using WE-AI or CO2-CO2. The investigators will also assess the impact of these three methods on patients comfort and activities in the post-procedure period.

Key facts

Study ID: NCT02409979
Run by: Presidio Ospedaliero Santa Barbara
People needed: 246
Starts: 2015-04-01
Expected to finish: 2015-11-01
Last updated by the study team: 2015-11-05

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

consecutive 18 to 80 year-old first-time diagnostic outpatients agreeing to start procedure without premedication

You may not qualify if…

patient unwillingness to start the procedure without sedation/analgesia
previous colorectal surgery
proctosigmoidoscopy or bidirectional endoscopy
patient refusal or inability to provide informed consent
inadequate consumption of bowel preparation
moderate or severe chronic obstructive pulmonary disease requiring oxygen
medical history of CO2 retention
history of inflammatory bowel disease

Where it is running

Sepulveda Ambulatory Care Center, VA Greater Los Angeles Healthcare System — Los Angeles, California, United States
Digestive Diseases Center, Vìtkovice Hospital — Ostrava, Czechia
Digestive Endoscopy Unit, Ospedale S. Barbara — Iglesias, CI, Italy

Full record on ClinicalTrials.gov

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