CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 41 enrolled
Drug / intervention
[18F]Flutemetamoldrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02778971
NCT02778971N/ACompleted

Implications for Management of PET Amyloid Classification Technology

University of Utah·observational·Posted May 20, 2016·Updated Apr 24, 2023

In Brief

An observational study evaluating [18F]Flutemetamol for Mild Cognitive Impairment and 2 related conditions. Completed, enrolled 41 participants across 1 site.

Detailed Summary

The main purpose of this study is to explore the impact of an amyloid positron emission tomography and computed tomography (PET/CT) scan on physician diagnosis and management, including drug management and care practices, for patients with a diagnosis of cognitive impairment. This study also intends to capture specific patient-reported outcomes related to patient burden, confidence and satisfaction. The hypothesis is that to aid early diagnosis, individuals with a diagnostically uncertain etiology for their dementia will benefit from knowledge of amyloid plaque burden status, through an alteration of patient diagnosis and management, which will lead to significant changes in patient and care partner reported outcomes.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedMay 20, 2016
Enrollment StartJun 1, 2016
Primary CompletionJun 1, 2018
Study CompletionSep 1, 2022
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 10.1 years ago

Interventions

[18F]Flutemetamoldrug

amyloid PET imaging with \[18F\]Flutemetamol and subsequent modification of diagnosis and management