Memory and Attention Problems in Lupus: New Treatment Trial With Modafinil
Information source: Hospital for Special Surgery, New York
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Systemic Lupus Erythematosus
Intervention: Modafinil (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Hospital for Special Surgery, New York Official(s) and/or principal investigator(s): Melanie J. Harrison, MD, MS, Principal Investigator, Affiliation: Hospital for Special Surgery
Overall contact: Debbie Miller, BA, Phone: 212-606-1867, Email: millerd@hss.edu
Summary
This study is being conducted in order to determine if the FDA-approved drug Modafinil can
improve cognitive function in patients with lupus. Modafinil is currently being used to
treat excessive sleepiness caused by certain sleep disorders. It has also been shown to
improve attention and concentration in some people who don’t have lupus or sleep disorders.
This study hopes to determine if Modafinil can be used safely and effectively in lupus
patients, and improve their quality of life. No medications currently exist for the treatment
of lupus-associated cognitive dysfunction.
Clinical Details
Official title: Pilot and Feasibility Study of Modafinil Treatment to Improve Cognitive Efficiency in SLE Patients
Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Primary outcome: Improvement in cognitive efficiency at 6 weeks
Secondary outcome: Change in performance of cognitive activities at six weeksChange in fatigue at six weeks Change in sleep at six weeks Adverse events, including an increase in SLE activity, at six weeks
Detailed description:
This is a 6-week pilot and feasibility single-arm, open-label trial of modafinil 200mg orally
every morning to improve cognitive efficiency in systemic lupus patients with cognitive
difficulties in daily life.
Cognitive dysfunction is a well-recognized manifestation of systemic lupus erythematosus
(SLE) whose reported prevalence ranges from 12-87%. SLE-associated cognitive dysfunction
often occurs in the absence of frank neuropsychiatric disease (e. g., stroke, depression,
psychosis, cerebral vasculitis), medications known to have central nervous system effects, or
increased disease activity or flare. Studies of SLE antibodies (most notably the
antiphospholipid antibodies) have provided conflicting results with respect to their
association with SLE-associated cognitive dysfunction. Thus, despite numerous
investigations, the etiology of SLE-associated cognitive dysfunction remains unclear. There
is no known means for preventing cognitive dysfunction in SLE. Similarly there are no
established or proven treatments for cognitive dysfunction in SLE.
Regardless of its cause, course, or long-term consequences, cognitive dysfunction in SLE is a
major cause of distress, compromised performance of everyday activities, and decreased
quality of life. Thus, treatment of decreased cognitive performance in SLE when it occurs,
no matter how mild, and regardless of its potential for permanence or progression, is of
paramount importance. It is imperative to provide SLE patients with cognitive performance
difficulties with the means to functionally cope with their impairments so that they can
maintain, if not regain their independence.
Modafinil is a safe, orally administered wakefulness-promoting agent approved for use in
adults suffering from narcolepsy, idiopathic hypersomnia, obstructive sleep apnea, and shift
work sleep syndrome. Since its FDA approval, it has been used for many additional varied
conditions including depression, fatigue, fibromyalgia, myotonic dystrophy, organic brain
syndrome, sleep deprivation, Parkinson’s, and drug-induced somnolence. It has also been used
in helicopter and airplane pilots to enhance their attentiveness during long flights. Some
of our SLE patients have been prescribed modafinil for narcolepsy or associated fatigue.
Modafinil has broad efficacy in health and illness. It enhances cognitive function in normal
young adult males, as tested by digit span, visual pattern recognition memory, spatial
planning and stop-signal reaction time. While the majority of patients prescribed modafinil
received the drug for non-cognitive indications (e. g., fatigue, sleepiness), several have
reported improved cognitive function, especially with respect to tasks that require attention
and concentration.
We hypothesize that Modafinil, an FDA-approved, non-specific wakefulness-promoting agent with
minimal side effects, is safe and effective when used to improve cognitive efficiency in SLE
patients who identify cognitive dysfunction in themselves.
Eligibility
Minimum age: 18 Years.
Maximum age: 60 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Fulfill ACR Classification Criteria for SLE
- >18 and < 60 years old
- English-speaking/reading
- Has a treating rheumatologist at the Hospital for Special Surgery
- Estimated premorbid verbal I. Q. >80 measured by the North American Adult Reading Test
- Functional difficulties due to cognitive dysfunction defined as positive endorsement
of ≥6 items on the Cognitive Symptoms Inventory (CSI). The CSI is a 21-item,
self-report questionnaire designed to assess ability to perform everyday activities in
patients with rheumatic disease. 47
- No physical or mental disabilities that would preclude or confound the results of the
neuropsychological testing, e. g., compromised use of hands, severe visual or hearing
impairment
- Able to read normal newsprint and hear a normal speaking voice
- Normotensive at time of enrollment with or without medication
- No arrhythmia or left ventricular hypertrophy on ECG
- Adequate contraception (barrier method)
Exclusion Criteria:
- Global cognitive impairment as measured by a Modified Mini Mental Status<77
- History of arrhythmia; known history of left ventricular hypertrophy, mitral valve
prolapse with syndrome, or other significant cardiovascular disease with a reduced
ejection fraction
- Renal insufficiency (creatinine clearance < 30 ml/min) including dialysis patients
- Known liver disease (e. g., active hepatitis) or any liver function test >2x upper
limit of normal (transaminases or GGTP)
- Significant and serious SLE activity defined as active central nervous system disease,
active nephritis, ulcerative skin disease. Other active SLE-associated conditions
involving major organ systems may be excluded at the discretion of the investigator.
- Pregnancy, nursing mother, or unwillingness to use barrier contraception
- Diagnosis of active psychosis, ADHD, ADD
- Current use of medications contraindicated with the use of modafinil-triazolam,
Phenobarbital, cyclosporine A, theophylline, carbamazepine, diazepam, phenytoin,
mephenytoin, rifampin, ketoconazole, itraconazole,
- Illegal drug or alcohol abuse (defined as two affirmative responses to the CAGE
questionnaire)
- Prior use of modafinil
Locations and Contacts
Debbie Miller, BA, Phone: 212-606-1867, Email: millerd@hss.edu
Hospital for Special Surgery, New York, New York 10021, United States; Recruiting
Additional Information
Starting date: February 2006
Ending date: February 2007
Last updated: September 26, 2006
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