Clinical Trials Directory

Trials / Terminated

TerminatedNCT03008031

Reduced Contrast Administration in Contrast-enhanced Spectral Mammography (CESM)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
11 (actual)
Sponsor
Maastricht University Medical Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The optimal dose of iodine based contrast agents used in contrast-enhanced spectral mammography (CESM) is unknown. If CESM, performed with lower dose of iodine based contrast agent, visualizes a tumor comparable to CESM with regular dose of contrast agent, patients can receive less contrast agent for CESM in future and thereby risking less side effects of the contrast agent. In order to study whether CESM remains unchanged at smaller amounts of contrast administration, a second CESM exam will be performed within one week of the first with a an alternative amount of contrast, it being either 80%, 60% or 40% of the original contrast dose. The settings of the CESM unit will remain unchanged.

Conditions

Interventions

TypeNameDescription
PROCEDURECESM with a reduced dose of contrast agent

Timeline

Start date
2017-01-01
Primary completion
2020-04-01
Completion
2020-04-01
First posted
2017-01-02
Last updated
2022-09-13

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT03008031. Inclusion in this directory is not an endorsement.