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.

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. - Oral contrast agents in patients undergoing contrast-enhanced abdominal CT.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON44229

Enrollment

200

Registered

2017-11-28

Start date

2017-12-04

Completion date

Unknown

Last updated

2024-04-15

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

Conditions

not applicable

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo an abdominal CT with oral contrast at the department of Radiology; Outpatients; > 18 years.

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Primary parameters: quality of the scans and the diagnostic confidence by the radiologist.	—

Secondary

Measure	Time frame
Secondary parameters: patients discomfort and radiation exposure.	—

Countries

Netherlands

Outcome results