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A Study of EGb 761® (Tanakan®) in Dementia of Alzheimer Type Onset in Patients Suffering From Memory Complaints

This study has been completed.
Information provided by:
Ipsen Identifier:
First received: January 12, 2006
Last updated: December 14, 2009
Last verified: December 2009
The purpose of this study is to determine whether Tanakan® is effective at slowing the progression from memory complaint to dementia of Alzheimer's type.

Condition Intervention Phase
Memory Disorders, Age-Related Retention Disorders, Cognitive Drug: EGb 761® (Tanakan®) Other: Placebo Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: Efficacy and Tolerance of EGb 761® 120mg Two Times a Day on Dementia of Alzheimer Type's Onset in Patients Suffering From Memory Complaints. A Randomised, Double-blind, Multicentre, Parallel Groups, Placebo Controlled Phase IIIb/IV Study in Elderly Over 70

Resource links provided by NLM:

Further study details as provided by Ipsen:

Primary Outcome Measures:
  • EGb 761® efficacy on conversion rate of memory complaint to dementia of Alzheimer type by a survival analysis [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]

Secondary Outcome Measures:
  • Efficacy on rate of cognitive abilities decline [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]
  • Effect on concomitant diseases [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]
  • Concomitant treatments' reports [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]
  • Global evaluation of memory complaint by the patient [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]
  • Clinical safety [ Time Frame: Baseline, month 12, 24, 36, 48 and 60 ]

Enrollment: 2878
Study Start Date: February 2002
Study Completion Date: November 2009
Primary Completion Date: November 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1 Drug: EGb 761® (Tanakan®)
120 mg, 1 tablet twice a day, oral route, during 5 years.
Placebo Comparator: 2 Other: Placebo
1 tablet twice a day, oral route, during 5 years.


Ages Eligible for Study:   70 Years and older   (Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Spontaneously reporting a memory complaint
  • Short anxiety battery test < 6, (only if patient screened at GP site)
  • Geriatric depression scale < 15
  • Mini-mental state (MMS) > 25 in GP's office (in hospital site MMS is done as complementary scale)

Exclusion Criteria:

  • Objective memory impairment
  • Clinician rated dementia staging system > 0.5
  • Mini-mental state < 25
  • Dementia, past history of seizures, Parkinson disease
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00276510

  Show 700 Study Locations
Sponsors and Collaborators
Study Director: Phillippe Garnier, MD Ipsen
  More Information

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Pr B Vellas, Hospital La Grave Casselardit 170 av de Casselardit 31300 Toulouse Identifier: NCT00276510     History of Changes
Other Study ID Numbers: 2-31-00240-011
Study First Received: January 12, 2006
Last Updated: December 14, 2009

Additional relevant MeSH terms:
Memory Disorders
Alzheimer Disease
Pathologic Processes
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurocognitive Disorders
Mental Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Signs and Symptoms
Neurodegenerative Diseases processed this record on September 21, 2017