Efficacy and Tolerability of Memantine in Frontotemporal Dementia (FTD) Patients

NCT00200538 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2013-05-03

No results posted yet for this study

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

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00200538 on ClinicalTrials.gov