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A Phase III Open-Label Extension Study Of Gabapentin As Adjunctive Therapy In Japanese Pediatric Patients With Partial Seizures
This study is currently recruiting participants.
Verified by Pfizer, December 2008
Sponsored by: Pfizer
Information provided by: Pfizer
ClinicalTrials.gov Identifier: NCT00620555
  Purpose

Examine the safety and efficacy of gabapentin as adjunctive therapy in Japanese pediatric patients with partial seizures


Condition Intervention Phase
Epilepsies, Partial
Drug: gabapentin
Phase III

Genetics Home Reference related topics: autosomal dominant partial epilepsy with auditory features pyridoxal 5'-phosphate-dependent epilepsy pyridoxine-dependent epilepsy
MedlinePlus related topics: Epilepsy Seizures
Drug Information available for: Gabapentin
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Single Group Assignment, Safety/Efficacy Study
Official Title: A 52 Weeks, Open-Label, Multicenter Study Evaluating The Efficacy And Safety Of Gabapentin As Adjunctive Therapy In Pediatric Patients Who Have Completed The 12 Weeks Treatment In Study A9451162

Further study details as provided by Pfizer:

Primary Outcome Measures:
  • Safety (adverse events, serious adverse events, withdrawals due to adverse events, results of clinical laboratory tests) [ Time Frame: 52 weeks ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Response Ratio, Responder Rate, Percent change in seizure frequency [ Time Frame: 52 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 80
Study Start Date: May 2008
Estimated Study Completion Date: August 2010
Estimated Primary Completion Date: August 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
gabapentin: Experimental Drug: gabapentin
Orally administered gabapentin

  Eligibility

Ages Eligible for Study:   3 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Completion of study A9451162

Exclusion Criteria:

  • Seizures related to drugs or acute medical illness
  • History of any serious medical or psychiatric disorder
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00620555

Contacts
Contact: Pfizer CT.gov Call Center 1-800-718-1021

Locations
Japan
Pfizer Investigational Site Not yet recruiting
Hiroshima, Japan
Pfizer Investigational Site Not yet recruiting
Saitama, Japan
Pfizer Investigational Site Not yet recruiting
Yamagata, Japan
Japan, Hyogo
Pfizer Investigational Site Recruiting
Kobe, Hyogo, Japan
Japan, Ishikawa
Pfizer Investigational Site Not yet recruiting
Kanazawa, Ishikawa, Japan
Japan, Miyagi-ken
Pfizer Investigational Site Recruiting
Sendai-shi, Miyagi-ken, Japan
Japan, Nagoya
Pfizer Investigational Site Recruiting
Showa-Ku, Nagoya, Japan
Japan, Niigata
Pfizer Investigational Site Recruiting
Niigata-shi, Niigata, Japan
Japan, Okayama
Pfizer Investigational Site Recruiting
Okayama-shi, Okayama, Japan
Japan, Osaka
Pfizer Investigational Site Recruiting
Suita, Osaka, Japan
Pfizer Investigational Site Recruiting
Izumi-shi, Osaka, Japan
Japan, Shizuoka
Pfizer Investigational Site Recruiting
Shizuoka-shi, Shizuoka, Japan
Japan, Tokyo
Pfizer Investigational Site Recruiting
Setagaya-ku, Tokyo, Japan
Pfizer Investigational Site Recruiting
Kodaira, Tokyo, Japan
Pfizer Investigational Site Not yet recruiting
Kiyose-shi, Tokyo, Japan
Pfizer Investigational Site Not yet recruiting
Shinjuku-ku, Tokyo, Japan
Sponsors and Collaborators
Pfizer
Investigators
Study Director: Pfizer CT.gov Call Center Pfizer
  More Information

To obtain contact information for a study center near you, click here.  This link exits the ClinicalTrials.gov site

Responsible Party: Pfizer, Inc. ( Director, Clinical Trials Disclosure Group )
Study ID Numbers: A9451165
Study First Received: February 11, 2008
Last Updated: December 23, 2008
ClinicalTrials.gov Identifier: NCT00620555  
Health Authority: Japan: Ministry of Health, Labor and Welfare

Study placed in the following topic categories:
Epilepsies, Partial
Excitatory Amino Acids
Calcium, Dietary
Gabapentin
Epilepsy
Seizures
Central Nervous System Diseases
Brain Diseases

Additional relevant MeSH terms:
Neurotransmitter Agents
Tranquilizing Agents
Molecular Mechanisms of Pharmacological Action
Anti-Dyskinesia Agents
Nervous System Diseases
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Depressants
Antiparkinson Agents
Calcium Channel Blockers
Excitatory Amino Acid Agents
Cardiovascular Agents
Antimanic Agents
Pharmacologic Actions
Membrane Transport Modulators
Sensory System Agents
Therapeutic Uses
Anti-Anxiety Agents
Analgesics
Peripheral Nervous System Agents
Central Nervous System Agents
Anticonvulsants
Excitatory Amino Acid Antagonists

ClinicalTrials.gov processed this record on January 16, 2009