Clinical Trials Directory

Trials / Terminated

TerminatedNCT05491902

Pilot PET Study of Regional Cerebral Protein Synthesis in Alzheimer's

Status
Terminated
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
University of Manchester · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Measuring the rate of cerebral protein synthesis (rCPS) may enable us to better-understand the progression of Alzheimer's Disease (AD). This study is using a new method of measuring rCPS non-invasively, and to offer new approaches to the assessment of new therapeutic strategies in clinical trials. Previous studies have established the utility of \[11C\]-Leucine PET to assess the rCPS. This study will use \[11C\]- Leucine PET to measure rCPS in AD patients versus age-matched and young healthy subjects to determine whether a measurable difference exists. The study will involve participants receiving up to two PET scans, a structural MRI scan. The PET scanning procedures will involve some withdrawal of blood samples. The ultimate goal of this proposal is to indicate new routes for treatment of AD.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TEST[C11] Leucine PET scanEach participant will receive an i.v. bolus of the PET radioligand, \[11C\]-Leucine (\<100 μg), for each scan. \[11C\]-Leucine is a PET radioligand has been used and studied clinically (17-23) at micro-doses (\<100 μg) with no adverse effects.
DIAGNOSTIC_TEST[18F] Flutemetamol PET scanEach participant will receive an i.v. bolus of the PET radioligand, \[18F\]-Flutemetamol (\< 10 μg), for each scan.
DIAGNOSTIC_TESTMRI scanScans will be performed on a 1.5T Philips scanner including a 3D T1-weighted scan for co-registration with PET scans and rating of hippocampal atrophy, as well as standard T1 and T2-weighted sequences for rating of white matter lesions.

Timeline

Start date
2017-10-09
Primary completion
2020-10-15
Completion
2020-10-15
First posted
2022-08-08
Last updated
2022-08-08

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT05491902. Inclusion in this directory is not an endorsement.