drugset / Trial / NCT06846853

Gadopiclenol vs. Gadobutrol for Dynamic Contrast-Enhanced Pituitary MRI (Magnetic Resonance Imaging)

NCT06846853

Phase 4 Recruiting 10 enrolled UConn Health
RandomizedCrossoverQuadruple-blindDiagnostic

Summary

This study will evaluate the efficacy and safety of Gadopiclenol, an FDA-approved contrast agent, for visualizing pituitary lesions on MR images by comparing with the comparator, Gadobutrol, a clinically widely used contrast agent. The study is double-blinded, so neither the participants nor the researchers know which contrast agent is being used during each scan to avoid the bias of results.

Timeline

Start
2025-03-25
Primary completion
2026-06-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Gadobutrol Diagnostic / imaging agent 0.1 unknown
Subject Gadopiclenol Diagnostic / imaging agent 0.05 unknown

Indications

No indication recorded.