Efficacy and Tolerability of Memantine in Frontotemporal Dementia (FTD) Patients
NCT00200538 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 52
Last updated 2013-05-03
Summary
The purpose of this trial is to assess the efficacy and tolerability of memantine (anti-excitotoxic, neuroprotective treatment currently used in Alzheimer's disease \[AD\]) in frontotemporal dementia patients after a one-year treatment.
Conditions
Interventions
- DRUG
-
memantine
Sponsors & Collaborators
-
Nantes University Hospital
lead OTHER
Principal Investigators
-
Martine Vercelletto, MD · Centre de la Mémoire, Clinique Neurologique CHU Nord Nantes 44093 France; [email protected]
-
Lucette Lacomblez, MD · Federation de Neurologie AP-HP Paris 75 013 France; [email protected]
-
Bruno Dubois, MD · Centre du Langage et de Neuropsychologie AP-HP Paris 75013 France; [email protected]
-
Anne Sophie Rigaud, MD · Hôpital Broca, Paris 75 France; [email protected]
-
Jean-Francois Dartigues, MD · Hôpital Pellegrin Bordeaux 33 076 France; [email protected]
-
Sophie Auriacombe, MD · Hôpital Pellegrin Bordeaux 33 076 France ; [email protected]
-
Philippe Couratier, MD · Hôpital Dupuytren, Limoges 87000 France; [email protected]
-
Jacques Touchon, MD · Hôpital Gui de Chaulliac, Montpellier 34 295 France; [email protected]
-
Matthieu Ceccaldi, MD · Hôpital de la Timone Marseille 13 005 France; [email protected]
-
Mira Didic, MD · Hôpital de la Timone Marseille 13005 France; [email protected]
-
Serge Bakchine, MD · Hôpital Maison Blanche, Reims 51 092 France; [email protected]
-
Bernard-Francois Michel, MD · Hôpital Sainte Marguerite, 13009 France; [email protected]
-
Catherine Thomas-Anterion, MD · Hôpital Bellevue Saint Etienne, 42 000 France; [email protected]
-
Bernard Laurent, MD · Hôpital Bellevue Saint Etienne 42 000 France; [email protected]
-
Francois Sellal, MD · Hôpital Civil Strasbourg 67000 France; [email protected]
-
Serge Belliard, MD · Hôpital Pontchaillou Rennes 35 000, France; [email protected]
-
Herve Allain, MD · Service de Pharmacologie, CHU de Rennes 35 000 France ; [email protected]
-
Michele Puel, MD · Hôpital Purpan, Toulouse 31059 France; [email protected]
-
Jean-Francois Demonet, MD · Clinique Neurologique CHU Purpan Toulouse 31059 France; [email protected]
-
Marie Sarazin, MD · Centre du Langage et de la Mémoire, Hôpital de la Salpétriére AP-HP Paris 75013 France
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 45 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-09-30
Countries
- France
Study Locations
More Related Trials
-
Prediction of Cognitive Properties of Memantine for Neurodegenerative Diseases
NCT02288000 ·Status: TERMINATED ·Phase: PHASE1
-
The Use of Memantine for Prevention of Alzheimer's Disease
NCT05063851 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
The Effect of Memantine on Brain Structure and Chemistry in Alzheimer's Disease Patients
NCT00255086 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Memantine for Parkinson's Disease Dementia (PDD) and Dementia With Lewy Bodies (DLB)
NCT00630500 ·Status: COMPLETED ·Phase: PHASE2
-
Biomarker Predictors of Memantine Sensitivity in Patients With Alzheimer's Disease
NCT03703856 ·Status: COMPLETED ·Phase: PHASE4
-
Effects of Memantine on Magnetic Resonance (MR) Spectroscopy in Subjects at Risk for Alzheimer's Disease
NCT00933608 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Memantine in Assessment of Selected Measures of Volumetric Magnetic Resonance Imaging (MRI) and Cognition in Moderate AD (Alzheimer's Disease)
NCT00334906 ·Status: COMPLETED ·Phase: PHASE4
-
Amantadine for the Treatment of Behavioral Disturbance in Frontotemporal Dementia (FTD)
NCT00127114 ·Status: WITHDRAWN ·Phase: PHASE4
-
Efficacy and Safety of Memantine in Moderate to Severe Alzheimer's Disease
NCT00857649 ·Status: TERMINATED ·Phase: PHASE3
-
Memantine Hydrochloride for Treatment of Cognitive Dysfunction Due to Traumatic Brain Injury
NCT06337994 ·Status: COMPLETED ·Phase: PHASE3
-
Investigation of Memantine in the Treatment of Memory, Concentration or Attention Problems
NCT01261741 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of DNL593 in Healthy Participants and Participants With Frontotemporal Dementia (FTD-GRN)
NCT05262023 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Safety and Tolerability of Memantine in Moderate to Severe Alzheimer's Disease
NCT00857233 ·Status: TERMINATED ·Phase: PHASE3
-
A Phase 2 Study to Evaluate Safety of Long-term AL001 Dosing in Frontotemporal Dementia (FTD) Patients (INFRONT-2)
NCT03987295 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluation of Memantine Versus Placebo on Ischemic Stroke Outcome
NCT02535611 ·Status: COMPLETED ·Phase: PHASE3
-
Open Label Pilot Study of the Effects of Memantine on FDG-PET in Frontotemporal Dementia
NCT00594737 ·Status: COMPLETED ·Phase: PHASE3
-
MK0249 for the Symptomatic Treatment of Alzheimer's Disease (MK0249-011)
NCT00420420 ·Status: COMPLETED ·Phase: PHASE2
-
A 52 Week Open Label Trial of Memantine for Frontotemporal Lobar Degeneration
NCT00187525 ·Status: COMPLETED ·Phase: PHASE4
-
A Study Of PF-04447943 Compared To Placebo In Subjects With Mild To Moderate Alzheimer's Disease
NCT00930059 ·Status: COMPLETED ·Phase: PHASE2
-
Effect of Memantine on Functional Communication in Patients With Alzheimer's Disease
NCT00469456 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy Study of AC-3933 in Adults With Mild to Moderate Alzheimer's Disease
NCT00359944 ·Status: COMPLETED ·Phase: PHASE2
-
The Efficacy of a Combination Regimen in Patients With Mild to Moderate Probable Alzheimer's Disease
NCT01921972 ·Status: COMPLETED ·Phase: PHASE4
-
A Pilot Clinical Trial Of Memantine for Essential Tremor
NCT00439699 ·Status: COMPLETED ·Phase: PHASE4
-
Positron Emission Tomography (PET) Amyloid Imaging of the Brain in Healthy Young Adult Subjects
NCT01265394 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of T-817MA in Patients With Mild to Moderate Alzheimer's Disease (US202)
NCT02079909 ·Status: COMPLETED ·Phase: PHASE2