Abstract | OBJECTIVE: METHOD: A randomized, parallel-group, double-blind, placebo-controlled, fixed-dose, add-on study was conducted over 12 weeks. Forty patients with persistent symptoms after at least 6 months of stable antipsychotic treatment received E-EPA or placebo, in addition to their existing treatment. RESULTS: At 12 weeks, the E-EPA group had significantly greater reduction of Positive and Negative Syndrome Scale total scores and of dyskinesia scores than the placebo group. CONCLUSIONS: EPA may be an effective and well-tolerated add-on treatment in schizophrenia.
|
Authors | Robin Emsley, Christo Myburgh, Pieter Oosthuizen, Susan J van Rensburg |
Journal | The American journal of psychiatry
(Am J Psychiatry)
Vol. 159
Issue 9
Pg. 1596-8
(Sep 2002)
ISSN: 0002-953X [Print] United States |
PMID | 12202284
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antipsychotic Agents
- Placebos
- Eicosapentaenoic Acid
|
Topics |
- Adolescent
- Adult
- Antipsychotic Agents
(therapeutic use)
- Chronic Disease
- Double-Blind Method
- Drug Therapy, Combination
- Eicosapentaenoic Acid
(therapeutic use)
- Humans
- Middle Aged
- Placebos
- Psychiatric Status Rating Scales
- Schizophrenia
(diagnosis, drug therapy)
- Severity of Illness Index
- Treatment Outcome
|