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UnknownN/A

Applying Non-invasive Brain Stimulation in Alzheimer's Rehabilitation

Presently, few studies have evaluated the clinical impact of rTMS in Alzheimer's disease. Though some studies have demonstrated an improvement, there have been conflicting results, as others do not seem to demonstrate beneficial effects.

Rovereto, Trento, ItalyView details
UnknownPhase 2

Efficacy and Safety of the PET Imaging Agent [18F]NAV4694 in Subjects With Probable Alzheimer's Disease

This is a phase 2, open-label, multiple-center, non-randomized single dose study to assess the safety and efficacy of \[18F\]NAV4694 PET imaging in detecting beta-amyloid plaque in the brain in subjects with probable AD compared with health

New Haven, Connecticut, United States+6 moreView details
CompletedPhase 2

24-week Open-label Extension Study Evaluating PXT00864 Effect in Mild AD Patients Further to PLEODIAL-I Completion

PLEODIAL-II study is an extension of the previous pilot PLEODIAL-I study (CLN-PXT00864-03 protocol) and is designed for the descriptive analysis of patients with mild AD who are exposed to PXT00864 over an additional 24-week period.

Bordeaux, France, FranceView details
Active, not recruitingN/A

Behavioral Change Following Alzheimer's Disease (AD) Biomarker Disclosure

The proposed project will assess long-term changes to health/lifestyle, advanced planning, and research engagement that Black and White patients with Amnestic Mild Cognitive Impairment (aMCI) make following disclosure of positron emission t

Ann Arbor, Michigan, United StatesView details
CompletedPhase 1

Evaluation of [18F]RO6958948 as Tracer for Positron Emission Tomography (PET) Imaging of Tau Burden in Alzheimer's Disease Participants

This is a longitudinal, follow-up study in participants with Alzheimer's disease (AD) who previously participated in study BP29409 (NCT02187627). This study is designed to assess the longitudinal change of Tau pathology in the brain of part

Baltimore, Maryland, United StatesView details
TerminatedN/A

Treating Alzheimer's and Dementia With D-ribose

To study the effectiveness of d-ribose in treating Alzheimer's and Dementia

Kailua, Hawaii, United StatesView details
CompletedPhase 1

Tolerability and Safety of Subcutaneous Administration of AFFITOPE AD02 in Mild to Moderate Alzheimer's Disease

The purpose of this study is to assess the tolerability and safety of repeated subcutaneous injection of a single dose of AFFITOPE AD02 in patients with mild to moderate Alzheimer's Disease.

Vienna, AustriaView details
CompletedPhase 1 / Phase 2

Activity of AVE1625 in Mild to Moderate Alzheimer's Patients.

Primary: This study is being conducted to evaluate if AVE1625 is safe and tolerated in patients with Alzheimer's disease that is not too severe. There is also evaluation of whether patients who take the study medication improve compared to

Bridgewater, New Jersey, United States+4 moreView details
CompletedPhase 1

A Study to Assess Regional Cerebral Blood Flow as an Alzheimer's Disease Biomarker Compared to Positron Emission Tomography in Patients With Mild-to-Moderate Alzheimer's Disease and Cognitively Normal Elderly Subjects (Study MK-0000-068)(COMPLETED)

The aim of the study is to determine if regional cerebral blood flow, measured by dynamic arterial spin labeling (dASL), can be a biomarker for stage of Alzheimer's disease. The study is designed to be conducted in 2 parts in participants w

Multiple locationsView details
Unknown

Comparative Study Between Alzheimer's and Multi-infarct Dementia

Dementia is a neurological disease that causes cognitive and behavioral impairments that could ultimately interfere with the ability to function at work or to do the usual daily activities. It is recognized as a healthcare and social burden

Asyut, EgyptView details
CompletedPhase 1

Sodium-glucose Co Transporter 2 (sGLT2) Inhibitor and Endogenous Ketone Production

Background: The drug empagliflozin treats diabetes. It lowers blood sugar by increasing glucose the kidneys excrete.

Baltimore, Maryland, United StatesView details
Active, not recruitingPhase 2

Safety and Efficacy of Plasma Transfusion From Exercise-trained Donors in Patients With Early Alzheimer's Disease

Introduction Given that exercise training reduces the risk of developing Alzheimer's disease (AD), induces changes in the blood composition and has widespread systemic benefits, it is reasonable to hypothesize that exercised plasma may have

Trondheim, NorwayView details
RecruitingN/A

Blood-based Biomarkers for Diagnosis of Alzheimer's

Alzheimer's disease (AD) may currently be diagnosed using molecular biomarkers in cerebrospinal fluid (CSF) and/or positron emission tomography (PET). These diagnostic procedures are highly accurate, but the high cost and low availability h

Stavanger, NorwayView details
CompletedN/A

Exercise Trial for Alzheimer's Disease

Exercise Trial for Alzheimer's Disease(EXTRA) is a pilot randomized clinical trial involving a physcial activity program versus a healthy lifestyle program, with one year follow-up in 30 non-disabled, community-dwelling persons, age 65 and

Baton Rouge, Louisiana, United States+1 moreView details
CompletedN/A

A Four Month Home Based tDCS Study on Patients With Alzheimer's Disease.

The study is an open label study on patients with Alzheimer's dementia using home based transcranial direct current (tDCS) stimulation. Aims of the study is to investigate applicability and effect of treatment.

Tromsø, Troms, NorwayView details
CompletedN/A

Alzheimer's Disease and Physiological, Cognitive Function and BDNF Levels of Plasma Adaptation After Exercise Training

Alzheimer's disease (AD) is a neurodegenerative disease leading to one of the most common forms of dementia in humans and memory disorder is one of the first symptoms that lead to diagnosis.

Fort-de-France, MartiniqueView details
SuspendedPhase 2

The Dose Finding Study of DAOIB Added to tDCS for AD

This is a 26-week randomized, double-blind, placebo-controlled trial. We will enroll patients with aMCI or mild AD.

Kaohsiung City, TaiwanView details
RecruitingPhase 2

A Study to Assess the Efficacy and Safety of ML-007C-MA for the Treatment of Alzheimer's Disease Psychosis

ML-007C-MA-221 is a Phase 2, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of ML-007C-MA in male and female participants aged 55 to 90 years with hallucinations and delusions associated with Alzheime

Phoenix, Arizona, United States+25 moreView details
TerminatedPhase 2

Imaging Tau in Alzheimer's Disease and Normal Aging

This study is being done to learn about tau tangles in Alzheimer's disease. A type of PET scan is used to measure the abnormal accumulation of protein called tau in the brain.

New York, New York, United StatesView details
CompletedPhase 2

Study Evaluating Safety, Tolerability, And Immunogenicity Of ACC-001 In Subjects With Mild To Moderate Alzheimer's Disease

To assess the safety, tolerability, and immunogenicity of ACC-001, an investigational active immunization, in patients with mild to moderate Alzheimer's disease.

Paris, Cedex 13 (mri), France+23 moreView details
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