Effects of Treating Obstructive Sleep Apnea in Epilepsy

This study has been completed.
Sponsor:
Collaborator:
Information provided by:
Vanderbilt University
ClinicalTrials.gov Identifier:
NCT00047463
First received: October 7, 2002
Last updated: March 31, 2011
Last verified: March 2011

October 7, 2002
March 31, 2011
September 2002
July 2008   (final data collection date for primary outcome measure)
CPAP Adherence/Tolerance as Measured by Proportion of Nights [ Time Frame: 10 weeks ] [ Designated as safety issue: No ]
This measure quantifies how well patients use their CPAP. The standard unit of measurement is proportion of nights that the CPAP is used by a participant. Data were downloaded by a card placed in the CPAP machine reflecting use over the entire 10 weeks.
Not Provided
Complete list of historical versions of study NCT00047463 on ClinicalTrials.gov Archive Site
  • Ability to Blind CPAP [ Time Frame: 10 weeks ] [ Designated as safety issue: No ]
  • Need for One vs. Two Nights of Baseline Sleep Studies [ Time Frame: 1 night ] [ Designated as safety issue: No ]
  • Ability to Screen for Sleep Apnea With a Questionnaire [ Time Frame: 1 day ] [ Designated as safety issue: No ]
Not Provided
Not Provided
Not Provided
 
Effects of Treating Obstructive Sleep Apnea in Epilepsy
Effects of Treating Obstructive Sleep Apnea in Epilepsy

The purpose of this trial is to work out design issues prior to conducting a definitive phase 3 trial to determine whether treating sleep-related breathing disorders in people with epilepsy results in improvement in seizure control or an improvement in alertness during the day.

Despite appropriate treatment with medications, individuals with epilepsy often continue to have seizures, and many suffer from excessive daytime sleepiness and poor quality of life. Evidence from case studies suggests that treatment of coexisting obstructive sleep apnea (OSA)-stoppage in breathing during sleep-can reduce the frequency of seizures in people with epilepsy that is resistant to antiepileptic medication.

In this study, individuals with symptoms of OSA and 2 or more seizures a month who meet study criteria will undergo polysomnography, a test that continuously monitors normal and abnormal physiological activity during sleep. Those individuals who test positive for OSA will be randomized to either therapeutic or placebo continuous positive airway pressure (CPAP)-a mask treatment for sleep apnea-for 10 weeks, during which time seizure frequency, daytime sleepiness, health-related quality of life, and CPAP compliance will be assessed.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
  • Epilepsy
  • Sleep Apnea
  • Obstructive Sleep Apnea
  • Device: continuous positive airway pressure (CPAP)
    a mask treatment for sleep apnea
  • Device: Placebo-CPAP
    Placebo-CPAP
  • Active Comparator: 1
    continuous positive airway pressure (CPAP)
    Intervention: Device: continuous positive airway pressure (CPAP)
  • Placebo Comparator: 2
    Placebo-CPAP
    Intervention: Device: Placebo-CPAP

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
35
July 2008
July 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age of 18 years or older.
  • A history supportive of obstructive sleep apnea.
  • Subject is able and willing to provide informed consent and to cooperate with polysomnography.
  • Four or more quantifiable seizures per month.
  • Subjects and their physicians agree to have their medication regimens optimized so that they are on the best regimen titrated to therapeutic benefit prior to the baseline phase of the study.

Exclusion Criteria:

  • Seizures secondary to drugs, alcohol, infection, neoplasia, demyelination, metabolic illness, or progressive degenerative disease.
  • Non-epileptic spells (e.g., pseudoseizures) alone or in combination with epileptic seizures.
  • Narcolepsy or another primary sleep disorder that requires intervention with medications and which may affect results of study (e.g., severe periodic limb movement disorder).
  • Effectively treated OSA or prior exposure to continuous positive airway pressure.
  • History of poor compliance with antiepileptic medications.
  • Current treatment with the vagus nerve stimulator.
  • Pregnancy.
  • A significant history of medical or psychiatric disease which may impair participation in the trial.
  • A history of alcohol or drug abuse during the one-year period prior to trial participation.
  • Evidence of medical instability (e.g., congestive heart failure, cardiac arrhythmias, pulmonary disease) due to obstructive sleep apnea.
  • Subjects who are unaware of the majority of their seizures and lack a reliable witness.
  • Greater than ten seizures a day.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00047463
IRB030633, R01NS42698
Yes
Beth Malow/Professor of Neurology, Vanderbilt University
Vanderbilt University
National Institute of Neurological Disorders and Stroke (NINDS)
Principal Investigator: Beth Malow, M.D., M.S. Vanderbilt University
Vanderbilt University
March 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP