Effects of Armodafinil on Cognition for Patients With Schizophrenia or Schizoaffective Disorder
| Status: | Completed |
|---|---|
| Conditions: | Schizophrenia, Psychiatric |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 18 - 65 |
| Updated: | 10/14/2017 |
| Start Date: | August 2006 |
| End Date: | January 2010 |
Effect of Addition of Modafinil on the Tolerability and Efficacy for Cognition of Atypical Antipsychotic Drugs in Patients With Schizophrenia or Schizoaffective Disorder
This is a six week, double blind,placebo controlled study for patients with schizophrenia or
schizoaffective disorder treated with an atypical antipsychotic for at least two months.
Subjects will be randomized to take armodafinil (Nuvigil) or placebo along with their current
antipsychotic and tested at baseline and week 6 for differences in memory, attention and
problem-solving ability. Changes in weight during the six week study will also be tracked.
schizoaffective disorder treated with an atypical antipsychotic for at least two months.
Subjects will be randomized to take armodafinil (Nuvigil) or placebo along with their current
antipsychotic and tested at baseline and week 6 for differences in memory, attention and
problem-solving ability. Changes in weight during the six week study will also be tracked.
Inclusion criteria
- Men and women age 18-65 years
- Patients with DSM-IV defined schizophrenia or schizoaffective disorder
- Treated with any atypical antipsychotic for at least 2 months
- Patients with documented weight gain > 7% with current antipsychotic medication
- Able to provide written consent
Exclusion criteria
- Women who are pregnant or nursing. Female participants must have a negative urine
pregnancy test at screening.
- DSM-IV defined substance or alcohol dependence within the 2 months preceding the start
of the trial
- Treatment with a monoamine oxidase inhibitor (e.g., tranylcypromine, phenelzine,
isocarboxazid) within 2 weeks of starting the trial
- Patients considered at high risk for suicide or violence
- Patients with history of or symptoms on systems review consistent with clinically
significant and currently relevant hematologic, renal, hepatic, gastrointestinal,
endocrine, pulmonary, dermatologic, oncologic or neurologic (including seizures or
epilepsy) disease
- Patients with a history of or symptoms on systems review consistent with significant
cardiovascular disease, bypass surgery, or concurrent cardiovascular disease,
including uncontrolled hypertension, hypotension, congestive heart failure, angina
pectoris, or recent (within last 6 months) myocardial infarction
- Use of any investigational drug within 4 weeks before screening
- History of hypersensitivity or other intolerable adverse effects to modafinil
- Patients who experience severe sleep disturbances from modafinil
We found this trial at
1
site
1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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