Skip to content

Carbon Dioxide During Screening Unsedated Colonoscopy

Randomized Clinical Trial to Compare Air Versus Carbon Dioxide in Screening Unsedated Colonoscopy.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01461564
Enrollment
200
Registered
2011-10-28
Start date
2010-01-31
Completion date
2011-06-30
Last updated
2014-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polyps

Keywords

screening, colonoscopy, carbon dioxide, air, pain score, complications

Brief summary

Colonoscopy is currently most effective procedure used for detecting colon cancer especially in the early stages. Screening colonoscopies are performed in the symptom-free patients at risk of familial colon cancer. During colonoscopy air commonly used to insufflate the bowel may be retained after the procedure causing pain and discomfort to the patients. One of the methods used to reduce pain and discomfort is insufflation of carbon dioxide (CO2) instead of air during colonoscopy. Aim of the study is evaluation of the use of carbon dioxide insufflation during colonoscopy.

Detailed description

The study was conducted in 200 consecutive patients undergoing screening colonoscopies for the detection of early colon cancer. The examinations were performed with Olympus 165 colonoscopes by seven experienced endoscopists, each of whom performed alone about over 2000 colonoscopies. The patients were randomly assigned to Group I and II with either air or carbon dioxide insufflation. Both study groups were matched by sex, age, duration of the procedure, and BMI. The authors compared for the duration of the procedure, coecal intubation time, complication rate, pulse rates immediately after the procedure, 15 minutes after, and subjective pain evaluation on a Visual Analogue Scale.

Interventions

PROCEDUREColonoscopy

Screening colonoscopy

Sponsors

Jagiellonian University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
50 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* age 50 yo and more * no previous large bowel operations * no previous colonoscopy * informed consent

Exclusion criteria

* previous colonoscopy * previous large bowel operations/ polypectomies

Design outcomes

Primary

MeasureTime frameDescription
duration of procedure1 hourTime from introduction of a colonoscope to removal of the colonoscope.

Secondary

MeasureTime frameDescription
coecal intubation time1 hourTime from introduction of a colonoscope to intubation of the coecumo
pain immediately after the procedure1 minPain assessed by VAS scale immediately after colonoscopy
pain 15 minutes after colonoscopy15 minPain assessed by VAS scale 15 minutes after colonoscopy
complication rate24 hoursany compication of screening colonoscopy

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026