Trial Condition(s):
Study to evaluate the diagnostic efficacy of Gd-EOB-DTPA in the characterization of focal liver lesions
90391
Not Available
Not Available
Please see attached Study Results Summary below.
No Inclusion Criteria Available
No Exclusion Criteria Available
Locations | Status |
---|
A multi-center (US) open-label study of Gd-EOB-DTPA with a single intravenous injection (25 μmol/kg body weight) in patients with known or suspected focal liver lesions and the corresponding blinded reading to evaluate the diagnostic efficacy of Gd-EOB-DTPA in the characterization of focal liver lesions
Trial Type:
Interventional
Intervention Type:
N/A
Trial Purpose:
N/A
Allocation:
N/A
Blinding:
N/A
Assignment:
N/A
Trial Arms:
N/A