Pharmacopsychiatry 2012; 45(05): 177-181
DOI: 10.1055/s-0031-1299769
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Efficacy and Tolerability of Ziprasidone vs. Olanzapine in Naive First-Episode Schizophrenia: A 6-Week, Randomized, Open-Label, Flexible-Dose Study

Authors

  • Y.-M. Li

    1   Mental Health Institute of The Second Xiangya Hospital Changsha, Central South University, Hunan, People’s Republic of China
    2   Department of Nursing of the Second Xiangya Hospital Changsha, Central South University, Hunan, People’s Republic of China
  • J.-P. Zhao

    1   Mental Health Institute of The Second Xiangya Hospital Changsha, Central South University, Hunan, People’s Republic of China
  • J.-J. Ou

    1   Mental Health Institute of The Second Xiangya Hospital Changsha, Central South University, Hunan, People’s Republic of China
  • R.-R. Wu

    1   Mental Health Institute of The Second Xiangya Hospital Changsha, Central South University, Hunan, People’s Republic of China
Further Information

Publication History

received 14 July 2011
revised 15 December 2011

accepted 28 December 2011

Publication Date:
30 January 2012 (online)

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Abstract

Introduction:

Although some previous studies have compared the 2 medicines, ziprasidone and olanzapine most selected chronic patients as subjects. Therefore, the present study was designed to compare the efficacy and safety of ziprasidone vs. olanzapine in naive first-episode schizophrenia.

Methods:

80 patients were randomly assigned to a 6-week treatment either with 80–160 mg/day of ziprasidone or 10–20 mg/day of olanzapine. The primary efficacy measurements were the Positive and Negative Syndrome Scale and Clinical Global Impression-severity scale scores. The second efficacy measurement was the response rate of treatment. Tolerability assessments were also performed.

Results:

79 patients completed the trial. The average dose was 127.5 mg/day with ziprasidone and 19.1 mg/day with olanzapine. No significant differences were found between the 2 groups in primary or secondary efficacy measurements at each visit point (all p>0.05). Body weight significantly increased with olanzapine, and more extrapyramidal symptoms were observed with ziprasidone (all p<0.05). Both medicines were well tolerated, and no serious adverse events were observed.

Conclusion:

Ziprasidone was as effective as olanzapine in short-term treatment for first-episode schizophrenia, and both medicines were well tolerated.