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Pharmacovigilance Study of Keppra. SPAIN - SKATE : Safety of Keppra as Adjunctive Therapy in Epilepsy
This study has been completed.
First Received: February 21, 2008   Last Updated: March 25, 2008   History of Changes
Sponsored by: UCB
Information provided by: UCB
ClinicalTrials.gov Identifier: NCT00643500
  Purpose

Patients with partial-onset seizures seen in community-based practices were to be included in this therapeutic use study

  • to assess the safety and tolerability of Keppra (Levetiracetam) and to confirm the favorable safety of the drug found during clinical development
  • to obtain further information about optimal dosing in daily clinical practice. Compared to previous registration trials, the study population corresponded more closely to that seen in daily clinical practice.

Condition Intervention Phase
Epilepsy, Partial
Drug: Levetiracetam
Phase IV

Genetics Home Reference related topics: autosomal dominant partial epilepsy with auditory features pyridoxal 5'-phosphate-dependent epilepsy
MedlinePlus related topics: Epilepsy Seizures
Drug Information available for: Levetiracetam
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study
Official Title: Pharmacovigilance Study of Keppra. SPAIN - SKATE : Safety of Keppra as Adjunctive Therapy in Epilepsy

Further study details as provided by UCB:

Primary Outcome Measures:
  • Adverse event rates, seizure counts and quality of life. [ Time Frame: 16 week treatment period ]

Enrollment: 342
Study Start Date: January 2002
Study Completion Date: May 2003
Primary Completion Date: May 2003 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   16 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male and female older than 16 years;
  • Epilepsy with partial onset seizures, with or without secondary generalization;
  • At least one concomitant marketed anti-epileptic drug

Exclusion Criteria:

  • Safety reasons
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00643500

Sponsors and Collaborators
UCB
Investigators
Study Director: UCB Clinical Trial Call Center +1 877 822 9493 (UCB)
  More Information

No publications provided

Responsible Party: UCB ( Study Director )
Study ID Numbers: N01033
Study First Received: February 21, 2008
Last Updated: March 25, 2008
ClinicalTrials.gov Identifier: NCT00643500     History of Changes
Health Authority: Spain: Spanish Agency of Medicines

Keywords provided by UCB:
Levetiracetam
Keppra

Study placed in the following topic categories:
Epilepsies, Partial
Nootropic Agents
Epilepsy
Central Nervous System Diseases
Etiracetam
Brain Diseases
Anticonvulsants

Additional relevant MeSH terms:
Epilepsies, Partial
Nootropic Agents
Epilepsy
Therapeutic Uses
Nervous System Diseases
Central Nervous System Diseases
Etiracetam
Brain Diseases
Central Nervous System Agents
Pharmacologic Actions
Anticonvulsants

ClinicalTrials.gov processed this record on May 07, 2009