Completed

Treatment Study for Frontotemporal Dementia

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Who is being recruted

Aphasia+17

+ Mental Disorders

+ Brain Diseases

From 45 to 95 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: July 2004
See protocol details

Summary

Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: July 23, 2004

Actual date on which the first participant was enrolled.

Objectives. The goal of the proposed clinical study is to assess the efficacy of a central nervous system stimulant and an atypical antipsychotic in treating the behavioral symptoms of FTD. Rationale. Frontotemporal dementia (FTD) is increasingly recognized as an important neuropsychiatric disorder. Symptoms of FTD include disinhibition, impulsivity, apathy, affective lability, and language dysfunction. The clinical syndrome is associated with frontal and/or anterior temporal atrophy on imaging and autopsy. Currently, no treatments have been proven to be effective for altering the course or clinical symptoms of FTD. Design. Study subjects will include 20 male and female patients with mild-moderate frontotemporal dementia recruited from participants in NINDS protocols 02-N-0001 and 81-N-0010. In a double-blinded crossover 11-week study without a placebo control, patients will be treated with a stimulant (dextroamphetamine) and an atypical antipsychotic (quetiapine). The primary outcome measures will be the Neuropsychiatric Inventory and the Clinical Global Impression of Change. Cognitive measures and side effects scales will also be collected.

Official TitleTreatment Study for Frontotemporal Dementia 
NCT00088751
Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

20 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 45 to 95 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

AphasiaMental DisordersBrain DiseasesCentral Nervous System DiseasesCommunication DisordersDementiaLanguage DisordersMetabolic DiseasesNervous System DiseasesNeurologic ManifestationsSpeech DisordersAphasia, Primary ProgressiveNeurodegenerative DiseasesNeurobehavioral ManifestationsNeurocognitive DisordersPick Disease of the BrainProteostasis DeficienciesFrontotemporal Lobar DegenerationTDP-43 ProteinopathiesFrontotemporal Dementia

Criteria

* INCLUSION CRITERIA: 1. FTD as diagnosed by the Lund-Manchester criteria including patients with diagnoses of Semantic Dementia or Primary Progressive Aphasia. 2. Ages 45 to 95 years old. 3. Mild-to-moderate (CDR 1 to 2) FTD with an assigned durable power of attorney. EXCLUSION CRITERIA: 1. Diagnosis of any form of dementia besides FTD, including AD, Lewy body dementia, vascular dementia, dementia associated with Parkinson's disease, Corticobasal Degeneration and Progressive Supranuclear Palsy. 2. Severe dementia (CDR 3). 3. Known allergy or serious adverse reaction to quetiapine or dextroamphetamine. 4. Patient is already receiving a stimulant (methylphenidate, dextroamphetamine, pemoline, or modafinil), or an antipsychotic medication, typical or atypical, including prochlorperazine and metoclopromide. 5. Patients taking any of the following medications because of their potential interaction with dextroamphetamine: MAO use currently or within 14 days prior to start of study, Furazolidone, Guanethidine, norepinephrine, sibutramine, tricyclic antidepressants, carbonic anhydrase inhibitors. 6. Patients taking the following medications because of their potential interaction with quetiapine: Carbamazepine, clozapine, lithium, thioridazine. 7. History of CVA, or at significantly increased risk for CVA (e.g., atrial fibrillation, recent TIA etc.). 8. Symptomatic cardiovascular disease (i.e., angina, claudication, TIAs, syncope), uncontrolled hyper or hypotension, or a tic disorder. 9. Any medical contraindication to performing the procedures involved in the study including blood draws or lumbar puncture. 10. We will require a woman of child-bearing age to have a pregnancy test prior to starting the study medications and to use contraception during the course of the study. 11. Patients with a previous negative trial of a stimulant. 12. Patients with a history of severe psychosis. 13. Patients with a history of recent substance abuse. 14. Patients with QTc prolongation on a baseline EKG. 15. A score of 2 or less on the Communication Functional Ratings - Swallowing Domain.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesSee the location
CompletedOne Study Center