Study to Evaluate Armodafinil Treatment in Improving Prefrontal Cortical Activation and Working Memory Performance

Trial ID or NCT#

NCT00711516

Status

not recruiting iconNOT RECRUITING

Purpose

The primary objective of this study is to determine whether treatment with armodafinil will provide improvements in prefrontal cortical activation in patients with OSAHS (Obstructive Sleep Apnea/Hypopnea Syndrome) who have residual sleepiness despite receiving nCPAP therapy.

Official Title

Double-Blind, Placebo-Controlled, Functional Neuroimaging Study of Armodafinil (200 mg/Day) on Prefrontal Cortical Activation in Patients With Residual Excessive Sleepiness Associated With Obstructive Sleep Apnea/Hypopnea

Eligibility Criteria

Ages Eligible for Study: 18 Years to 60 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - Patient has a current diagnosis of OSAHS and has a complaint of excessive sleepiness despite effective nCPAP therapy. - Patient has excessive sleepiness as evidenced by a mean sleep latency of less than 8 minutes, as determined by the MSLT. - Patient has an ESS score of 10 or more at the initial screening visit. - Patient has a habitual sleep time beginning no earlier than 2100 and ending no later than 0700. - Patient is right-handed. Patients who are ambidextrous may be eligible following consultation with the medical monitor. - Women of childbearing potential must use a medically accepted method of contraception and must agree to continue use of this method for the duration of the study and for 30 days after participation in the study. - Patient exhibits reasonable accuracy (≥80%) on the 2-back working memory task during the training session at the second screening visit.
Exclusion Criteria:
  1. The Patient: - The patient is a current smoker or has a prior history of smoking (defined as ≥1 pack-year) within 2 years prior to the screening visit. - consumes caffeine including coffee, tea and/or other caffeine-containing beverages or food averaging more than 400 mg of caffeine per day (approximately equivalent to 4 or more cups of coffee). - has NART-predicted verbal IQ and QIDS-SR16 scores within protocol-specific exclusionary ranges. - has a clinically significant, uncontrolled medical or psychiatric conditions (treated or untreated). - has a confirmed or probable diagnosis of a current sleep disorder other than OSAHS. - has used any excluded prescription drugs or procedures for prohibited and allowed drugs within the excluded timeframe. - has a history of alcohol, narcotic, or any other drug abuse. - has a positive UDS, without medical explanation, at the screening visit. - has a clinically significant deviation from normal in the physical examination. - is a pregnant or lactating woman. Any woman becoming pregnant during the study will be withdrawn from the study. - has a past or present seizure disorder, head trauma that is clinically significant, or past neurosurgery. - has used an investigational drug within 1 month before the screening visit. - has any disorder that may interfere with drug absorption, distribution, metabolism, or excretion (including gastrointestinal surgery). - has a known hypersensitivity to armodafinil or modafinil, or any other component of the study drug tablets. - has a history of any clinically significant cutaneous drug reaction, or a history of clinically significant hypersensitivity reaction, including multiple allergies or drug reactions. - has known human immunodeficiency virus (HIV). - has clinical laboratory test value(s) outside the range(s) specified in the Protocol, or presents a clinically significant laboratory abnormality without prior written approval by the medical monitor. - has worked the night shift within 28 days of the baseline visit, or will work the night shift during the double-blind segment of the study. - anticipates any travel across more than 3 time zones at any time during the study. - needs to use any of the excluded medications identified in this protocol. - is unable to complete neuroimaging studies, performance tasks, self-rating scales, and all other study assessments. - has a contraindication to fMRI scanning, (such as an implanted pacemaker/defibrillator, aneurysm clips, drug infusion device or metallic foreign body). - is suspected to be unable to tolerate fMRI scanning (eg, claustrophobic) and/or the testing paradigm. - has physical or other characteristics that suggest imaging data will be unobtainable or degraded.
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Investigator(s)

Clete A. Kushida, MD, PhD
Clete A. Kushida, MD, PhD
Sleep specialist, Neurologist
Professor of Psychiatry and Behavioral Sciences (Sleep Medicine)

Contact us to find out if this trial is right for you.

Contact

Chia-Yu Cardell
6507217576

View on ClinicalTrials.gov