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NCT01946243 · ClinicalTrials.gov registry record · Phase 4

The Feasibility of Florbetapir Quantitation

A Phase 4 study, sponsored by Avid Radiopharmaceuticals.

Completed
Registry status
Phase 4
Development phase
96
Enrollment target

NCT01946243: Completed Phase 4 study, sponsored by Avid Radiopharmaceuticals.

NCT01946243 is a Phase 4 study that has completed, run by Avid Radiopharmaceuticals. The registered enrollment target is 96 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01946243, a Phase 4 study, has completed, sponsored by Avid Radiopharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
96 participants
Enrollment target

Study Summary

The overall objective of the study is to assess the feasibility of implementing a quantitative process of florbetapir F 18 scan interpretation. The hypothesis is that the use of quantitative analysis will increase the accuracy of florbetapir F 18 scan interpretation.

Primary Outcome

Evaluate whether the addition of quantitation as an adjunct to qualitative interpretations (VisQ) significantly improved the total accuracy of Amyvid scan interpretation in lower accuracy readers. Only the 46 scans with autopsy from A07/A16 are used for this outcome measure.

Interventions

  • DRUG Florbetapir F18

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2013-08
Est. Completion 2014-04
Phase Phase 4
Avid Radiopharmaceuticals

42 total trials

What the finished NCT01946243 record still lists

NCT01946243 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 1 intervention - of which Florbetapir F18 is the first listed.

NCT01946243 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01946243 about?

NCT01946243 is a clinical study titled "The Feasibility of Florbetapir Quantitation". The overall objective of the study is to assess the feasibility of implementing a quantitative process of florbetapir F 18 scan interpretation. The hypothesis is that the use of quantitative analysis will increase the accuracy of florbetapir F 18 scan interpretation.

What is the current status of trial NCT01946243?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 96 participants. The study started on 2013-08. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01946243?

The interventions under investigation include: Florbetapir F18 (DRUG).

Who is sponsoring clinical trial NCT01946243?

This trial is sponsored by Avid Radiopharmaceuticals, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01946243's enrollment target sits among peer trials

96 863rd of 2000 higher than 1,132 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT01946243, the US trial registry maintained by the National Library of Medicine. NCT01946243 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.