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Completed Phase 3 Interventional Results available

Potential of Florbetapir F 18 PET to Inform Clinical Diagnosis and Management of Patients With Progressive Cognitive Decline

ClinicalTrials.gov ID: NCT01400425

Public ClinicalTrials.gov record NCT01400425. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 12:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study is designed to evaluate whether a florbetapir F 18 PET scan can impact clinical thinking when physicians are determining the likely cause of a subject's cognitive impairment.

Study identification

NCT ID
NCT01400425
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Avid Radiopharmaceuticals
Industry
Enrollment
239 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2011 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Mar 29, 2013

2011 – 2012

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Research Site Phoenix Arizona 85006 —
Research Site Sun City Arizona 85351 —
Research Site San Francisco California 94109 —
Research Site Boulder Colorado 80304 —
Research Site Boynton Beach Florida 33486 —
Research Site Clearwater Florida 33756 —
Research Site Fort Myers Florida 33912 —
Research Site West Palm Beach Florida 33407 —
Research Site Shreveport Louisiana 71130 —
Research Site Quincy Massachusetts 02169 —
Research Site Las Vegas Nevada 89121 —
Research Site New York New York 10021 —
Research Site Patchogue New York 11772 —
Research Site Durham North Carolina 27705 —
Research Site Greensboro North Carolina 27401 —
Research Site Providence Rhode Island 02903 —
Research Site Providence Rhode Island 02906 —
Research Site Houston Texas 77042 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01400425, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 29, 2013 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01400425 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →