At a glance
ClinicalIndex Comparison RecordN/ACompleted· 1,175 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Immediate Nausea and Vomiting After the Administration of Non-ionic Contrast Media: Prevalence and Risk Factors
In Brief
An observational study for Contrast Agent and Nausea. Completed, enrolled 1,175 participants across 1 site.
Detailed Summary
The prevalence of nausea and vomiting after the administration of non-ionic contrast media has rarely been assessed. Thus, the aim of our study is to evaluate the prevalence and risk factors of nausea and vomiting after the exposure to the non-ionic contrast media for computed tomography examinations in adults.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsContrast Agent, Nausea
CountriesSouth Korea
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartJan 2017
First PostedJan 2017
Primary CompletionMar 2017
TodayJul 2026
First PostedJan 12, 2017
Enrollment StartJan 1, 2017
Primary CompletionMar 31, 2017
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 9.5 years ago