A feasibility study comparing two strategies of oral contrast in patients undergoing contrast-enhanced abdominal CT: 50 ml Télébrix Gastro + 950 ml water vs 1000 ml water only.
Completed
- Conditions
- not applicable100179901001965410017991
- Registration Number
- NL-OMON44229
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
Patients scheduled to undergo an abdominal CT with oral contrast at the department of Radiology;
Outpatients;
> 18 years.
Exclusion Criteria
Patients undergoing CT for other research purpose;
Patients who are not willing to participate;
Not able to understand and/or give written informed consent
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary parameters: quality of the scans and the diagnostic confidence by the<br /><br>radiologist. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary parameters: patients discomfort and radiation exposure. </p><br>