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N/A Completed N=60

Evaluation of Transient Dyspnea During Gadoxetic Acid Enhanced Multiphasic Liver MRI

Source: ClinicalTrials.gov NCT02395991 ↗
Enrolled (actual)
60
Serious AEs
0.0%
Results posted
May 2021
Primary outcomePrimary: Number of Participants With Transient Dyspnea. — 23 Participants

Summary

The purpose of this study is to observe transient dyspnea pattern after Gd-EOB-DTPA administration by obtaining continuous dynamic T1 weighted image data.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Transient Dyspnea.
23
SECONDARY
Duration of Transient Dyspnea in Participants With Transient Dyspnea.
21.5

Eligibility Criteria

Inclusion Criteria

  • Patients who are referred to MR unit for hepatocyte-specific contrast enhanced liver MRI using gadoxetic acid, to characterize focal liver lesion or to investigate diffuse liver disease
  • OR, Liver living donor candidates
  • AND subjects who sign the informed consent.

Exclusion Criteria

  • Minors under 18 years old
  • All contraindication to MRI
  • Hypersensitivity to Gd
  • Biliary obstruction
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02395991). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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