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NCT01092546 · ClinicalTrials.gov registry record · Phase 3

Positron Emission Tomography Imaging of Brain Amyloid in Normal Pressure Hydrocephalus

A Phase 3 study, sponsored by GE Healthcare.

Terminated
Registry status
Phase 3
Development phase
12
Enrollment target

NCT01092546: Clinical Trial Phase 3 study, sponsored by GE Healthcare.

NCT01092546 is a Phase 3 study that was terminated before completion, run by GE Healthcare. The registered enrollment target is 12 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01092546, a Phase 3 study, was terminated before completion, sponsored by GE Healthcare.

TERMINATED
Registry status
Phase 3
Development phase
12 participants
Enrollment target

Study Summary

To determine the level of association between the quantitative estimates of brain uptake of \[18F\]flutemetamol and the quantitative immunohistochemical and histochemistry estimates of amyloid levels in frontal lobe biopsy samples obtained from subjects during shunt placement for NPH.

Primary Outcome

The level of association between the quantitative estimates of brain uptake of \[18F\]flutemetamol and the quantitative immunohistochemical estimates of amyloid levels in biopsy samples obtained during shunt placement in patients who have Normal Pressure Hydrocephalus (NPH). The quantitative estimates of brain uptake of \[18F\]flutemetamol (SUVR) will be made from the analysis of PET images.

Interventions

  • DRUG [18F]Flutemetamol

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2010-03
Est. Completion 2011-04
Phase Phase 3
GE Healthcare

99 total trials

Why NCT01092546 stopped before completion

NCT01092546 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which [18F]Flutemetamol is the first listed.

NCT01092546 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01092546 about?

NCT01092546 is a clinical study titled "Positron Emission Tomography Imaging of Brain Amyloid in Normal Pressure Hydrocephalus". To determine the level of association between the quantitative estimates of brain uptake of \[18F\]flutemetamol and the quantitative immunohistochemical and histochemistry estimates of amyloid levels in frontal lobe biopsy samples obtained from subjects during shunt placement for NPH.

What is the current status of trial NCT01092546?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 12 participants. The study started on 2010-03. Estimated completion is 2011-04.

What interventions are being tested in trial NCT01092546?

The interventions under investigation include: [18F]Flutemetamol (DRUG).

Who is sponsoring clinical trial NCT01092546?

This trial is sponsored by GE Healthcare, which has 99 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01092546's enrollment target sits among peer trials

12 1984th of 2000 higher than 12 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 NCT01092546, the US trial registry maintained by the National Library of Medicine. NCT01092546 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.