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NCT00323310 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of MultiHance in Pediatric Patients

A Phase 3 study, sponsored by Bracco Diagnostics.

Terminated
Registry status
Phase 3
Development phase
92
Enrollment target

NCT00323310: Clinical Trial Phase 3 study, sponsored by Bracco Diagnostics.

NCT00323310 is a Phase 3 study that was terminated before completion, run by Bracco Diagnostics. The registered enrollment target is 92 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00323310, a Phase 3 study, was terminated before completion, sponsored by Bracco Diagnostics.

TERMINATED
Registry status
Phase 3
Development phase
92 participants
Enrollment target

Study Summary

The purpose of this study was to assess the safety and enhancing properties of the magnetic resonance imaging (MRI) contrast agent MultiHance in children aged 2 to 17 years having central nervous system (CNS) disorders.

Primary Outcome

5-point scale (0=no delineation of lesion borders \[lesion not identified in image, lesion borders not visible\]; 1=poor border delineation \[all borders poorly distinct, lesion not separated from surrounding tissues/structures/edema\]; 2=moderate border delineation \[border delineation fair/not complete, lesion not clearly separated\]; 3=good border delineation \[border delineation complete, lesion adequately separated\]; 4=excellent border delineation \[borders sharply/clearly distinct, lesion

Interventions

  • DRUG gadobenate dimeglumine

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 2006-04
Est. Completion 2008-09
Phase Phase 3
Bracco Diagnostics

37 total trials

Why NCT00323310 stopped before completion

NCT00323310 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 92 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 1 intervention - of which gadobenate dimeglumine is the first listed.

NCT00323310 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00323310 about?

NCT00323310 is a clinical study titled "Safety and Efficacy of MultiHance in Pediatric Patients". The purpose of this study was to assess the safety and enhancing properties of the magnetic resonance imaging (MRI) contrast agent MultiHance in children aged 2 to 17 years having central nervous system (CNS) disorders.

What is the current status of trial NCT00323310?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 92 participants. The study started on 2006-04. Estimated completion is 2008-09.

What interventions are being tested in trial NCT00323310?

The interventions under investigation include: gadobenate dimeglumine (DRUG).

Who is sponsoring clinical trial NCT00323310?

This trial is sponsored by Bracco Diagnostics, which has 37 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00323310's enrollment target sits among peer trials

92 1723rd of 2000 higher than 277 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00323310, the US trial registry maintained by the National Library of Medicine. NCT00323310 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.