Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07040865

Randomized Comparison of Contrast Agents Gadopiclenol and Gadobutrol in the Workup of Incidental Renal and Adrenal Findings

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-11-19

104

Participants Needed

1

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to compare the effects of the contrast agent Gadopiclenol with those of the standard contrast agent Gadobutrol. The main question of this study is : Does gadopiclenol offer diagnostic properties that are equally effective as those of gadobutrol? Participants will be: * randomly assigned to one of two groups: the experimental group, which receives gadopiclenol, or the control group, which receives gadobutrol. Each participant is informed of their group allocation prior to the magnetic resonance imaging (MRI) scan. * invited for a single MRI appointment lasting approximately 60 minutes

CONDITIONS

Official Title

Randomized Comparison of Contrast Agents Gadopiclenol and Gadobutrol in the Workup of Incidental Renal and Adrenal Findings

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent
  • Age 18 years or older
  • Compatibility with magnetic resonance imaging
  • Planned workup of kidney or adrenal incidental findings (or both)
  • Body mass index (BMI) less than 31 kg/m2
Not Eligible

You will not qualify if you...

  • Presence of implants that might affect imaging parameters in the region under investigation
  • Vulnerable individuals
  • Claustrophobic individuals
  • Individuals cognitively impaired or unable to understand the language
  • Pregnant or breastfeeding patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Diagnostic, Interventional and Pediatric Radiology Inselspital, University of Bern

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

G

Grazia M. Cereghetti, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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