KCT0012407Active, not recruitingNot Applicable
MR Contrast Media Change for Reduction of Adverse Drug Reaction
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Asan Medical Center
- Enrollment
- 166
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Primary Purpose
- Treatment
Eligibility Criteria
- Ages
- 18(Year) to 80(Year) (—)
- Sex
- All
Inclusion Criteria
- •Patients aged 18 to 80 years.
- •Patients with a history of GBCA-related adverse drug reactions, classified as mild or moderate according to Korean clinical practice guidelines
- •Patients who are able to provide relevant information, including the type of GBCA associated with the previous reaction and the type and severity of the previous GBCA-related ADR.
- •Patients with a medical indication for contrast-enhanced MRI.
Exclusion Criteria
- •Patients who have experienced adverse reactions to two or more different GBCAs.
- •Patients whose previous GBCA-related adverse reaction was caused by gadoxetate disodium.
- •Patients who do not wish to receive premedication.
- •Patients who underwent contrast-enhanced CT or MRI within 24 hours before screening.
- •Patients for whom a specific GBCA has been designated by the Department of Allergy and Immunology.
- •Patients with a history of severe GBCA-related adverse reactions, including anaphylaxis, as defined by Korean clinical practice guidelines.
- •Patients requiring contrast agent administration through a central venous catheter.
Investigators
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