Status:

COMPLETED

Levetiracetam for Neuroprotection Against Corticosteroid-induced Hippocampal Dysfunction: A Proof of Concept Study

Lead Sponsor:

University of Texas Southwestern Medical Center

Collaborating Sponsors:

UCB Pharma

Conditions:

Memory Loss Associated With Corticosteroid Use

Manic State Associated With Corticosteroid Use

Eligibility:

All Genders

18-65 years

Phase:

PHASE4

Brief Summary

The purpose of this research is to determine whether the memory impairment and manic symptoms (feelings of agitation, overexcitement or hyperactivity) typically seen in those on corticosteroid therapy...

Eligibility Criteria

Inclusion

  • Age 18-65 years
  • Scheduled to receive a corticosteroid "burst" of at least 10 mg of prednisone equivalents and for at least 5 days duration
  • English- or Spanish-speaking

Exclusion

  • History of allergic reaction or other contraindication to levetiracetam therapy
  • Other unstable medical conditions (e.g. recent myocardial infarction, renal failure, diabetes with poor glycemic control)
  • Pregnant or nursing women
  • History of mental retardation, dementia or other severe cognitive disorders

Key Trial Info

Start Date :

February 1 2005

Trial Type :

INTERVENTIONAL

End Date :

November 1 2005

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT00223223

Start Date

February 1 2005

End Date

November 1 2005

Last Update

August 3 2011

Active Locations (1)

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Page 1 of 1 (1 locations)

1

The University of Texas Southwestern Medical Center

Dallas, Texas, United States, 75235

Levetiracetam for Neuroprotection Against Corticosteroid-induced Hippocampal Dysfunction: A Proof of Concept Study | DecenTrialz