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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT03141697 |
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Date of registration:
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26/04/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Use of CO2 in Routine-Colonoscopy
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Scientific title:
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Is CO2 Insufflation an Amelioration of Routine Colonoscopy? |
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Date of first enrolment:
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April 1, 2012 |
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Target sample size:
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150 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03141697 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Diagnostic. Masking: Triple (Participant, Care Provider, Investigator).
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Phase:
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N/A
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Countries of recruitment
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Germany
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- older than 18 years
- informed consent
Exclusion Criteria:
- former colonic resections
- severe heart or lung disease (NYHA III or IV)
- Pregnancy
- Patients with planned gastroscopy within 24 hours
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Colonoscopy
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Intervention(s)
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Device: Carbon Dioxide
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Device: Room air
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Primary Outcome(s)
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Post-procedural pain
[Time Frame: 0 - 24 hrs after colonoscopy]
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Secondary Outcome(s)
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procedure time
[Time Frame: duration of colonoscopy]
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Abdominal bloating
[Time Frame: 0 - 24 hrs after colonoscopy]
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flatulence
[Time Frame: 0 - 24 hrs after colonoscopy]
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Used amount of sedative drugs
[Time Frame: during endoscopy]
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Secondary ID(s)
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CO2 Colonoscopy
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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