Status:

COMPLETED

Efficacy of Fluoxetine in Reducing Ictal Hypoventilation in Patients With Partial Epilepsy

Lead Sponsor:

University of California, Davis

Conditions:

Uncontrolled Partial Epilepsy

Ictal Hypoventilation

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

The purpose of this study is to determine the effects of fluoxetine on breathing mechanisms during seizures. Patients with partial epilepsy commonly have changes in their breathing mechanisms during s...

Detailed Description

Patients who consent to participate in the study will come to the clinic one week prior to the scheduled date of hospitalization in the Epilepsy Monitoring Unit (EMU). At this visit a complete physica...

Eligibility Criteria

Inclusion

  • Adult patients with temporal lobe epilepsy, aged 18-65.
  • Medical intractability of seizures such that VET to determine candidacy for epilepsy surgery is determined to be clinically appropriate for the patient by the primary treating epileptologist.
  • Intelligence Quotient \>70.
  • Native English speaker or adequate fluency in English to provide informed consent.
  • Female patients of child-bearing potential must be using an acceptable method of contraception, including abstinence.

Exclusion

  • Progressive neurological disease.
  • Severe depression, bipolar disease or psychosis.
  • History of suicidal ideation or intent.
  • Clinically significant concurrent medical illness, including hepatic or renal insufficiency and diabetes.
  • Pregnant or lactating women.
  • Current heavy alcohol or illicit drug use.
  • Patients already taking fluoxetine or other selective serotonin reuptake inhibitors (SSRIs).
  • Concurrent use of monoaminoxidase inhibitors, antipsychotic agents, antidepressant agents other than SSRIs or frequent use of triptan agents.
  • History of a previous allergic reaction or adverse effects with SSRIs.
  • History of serotonin syndrome.

Key Trial Info

Start Date :

August 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2012

Estimated Enrollment :

2 Patients enrolled

Trial Details

Trial ID

NCT00986310

Start Date

August 1 2009

End Date

June 1 2012

Last Update

November 27 2019

Active Locations (1)

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1

University of California, Davis

Sacramento, California, United States, 95817