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Randomized clinical comparison of perospirone and risperidone in patients with schizophrenia: Kansai Psychiatric Multicenter Study
Aim: Perospirone is classified as a second‐generation antipsychotic agent for the treatment of schizophrenia. Perospirone binds with high affinity to serotonin 5‐HT2A receptors and dopamine D2 receptors. There are no reports of clinical comparisons of perospirone and risperidone in multicenter stud...
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Published in: | Psychiatry and clinical neurosciences 2009-06, Vol.63 (3), p.322-328 |
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container_title | Psychiatry and clinical neurosciences |
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creator | Okugawa, Gaku Kato, Masaki Wakeno, Masataka Koh, Jun Morikawa, Masayuki Matsumoto, Naoki Shinosaki, Kazuhiro Yoneda, Hiroshi Kishimoto, Toshifumi Kinoshita, Toshihiko |
description | Aim: Perospirone is classified as a second‐generation antipsychotic agent for the treatment of schizophrenia. Perospirone binds with high affinity to serotonin 5‐HT2A receptors and dopamine D2 receptors. There are no reports of clinical comparisons of perospirone and risperidone in multicenter studies. To clarify the clinical traits of perospirone in the treatment of schizophrenia, the clinical efficacies and side‐effects of perospirone and risperidone were compared in a randomized clinical multicenter trial.
Methods: Sixty‐six schizophrenia patients were enrolled in the trial. The Positive and Negative Syndrome Scale (PANSS) total, positive, negative and general symptoms scores and Drug‐Induced Extra‐Pyramidal Symptoms Scale (DIEPSS) scores were investigated at 0, 4, 8 and 12 weeks.
Results: Significant reductions in the PANSS total and subscale scores were observed in both the perospirone and risperidone groups, with no significant between‐group differences at 4 and 12 weeks. Risperidone improved the total scores and overall psychopathologic symptom total scores more effectively than perospirone at week 8. There were no significant differences in the DIEPSS scores at 0, 4, 8 and 12 weeks between the perospirone and risperidone groups. The numbers of patients who dropped out did not differ between the perospirone and risperidone groups.
Conclusions: Perospirone was as effective as risperidone against positive and negative symptoms in patients with schizophrenia. Both antipsychotic agents were equally well‐tolerated. |
doi_str_mv | 10.1111/j.1440-1819.2009.01947.x |
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Methods: Sixty‐six schizophrenia patients were enrolled in the trial. The Positive and Negative Syndrome Scale (PANSS) total, positive, negative and general symptoms scores and Drug‐Induced Extra‐Pyramidal Symptoms Scale (DIEPSS) scores were investigated at 0, 4, 8 and 12 weeks.
Results: Significant reductions in the PANSS total and subscale scores were observed in both the perospirone and risperidone groups, with no significant between‐group differences at 4 and 12 weeks. Risperidone improved the total scores and overall psychopathologic symptom total scores more effectively than perospirone at week 8. There were no significant differences in the DIEPSS scores at 0, 4, 8 and 12 weeks between the perospirone and risperidone groups. The numbers of patients who dropped out did not differ between the perospirone and risperidone groups.
Conclusions: Perospirone was as effective as risperidone against positive and negative symptoms in patients with schizophrenia. Both antipsychotic agents were equally well‐tolerated.</description><identifier>ISSN: 1323-1316</identifier><identifier>EISSN: 1440-1819</identifier><identifier>DOI: 10.1111/j.1440-1819.2009.01947.x</identifier><identifier>PMID: 19566763</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Adolescent ; Adult ; Adult and adolescent clinical studies ; Aged ; Antipsychotic Agents - adverse effects ; Antipsychotic Agents - therapeutic use ; antipsychotics ; Basal Ganglia Diseases - chemically induced ; Biological and medical sciences ; Female ; Humans ; Isoindoles - adverse effects ; Isoindoles - therapeutic use ; Male ; Medical sciences ; Middle Aged ; neuroleptic ; Neuropharmacology ; perospirone ; Pharmacology. Drug treatments ; Psychiatric Status Rating Scales - statistics & numerical data ; Psycholeptics: tranquillizer, neuroleptic ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychopharmacology ; Psychoses ; risperidone ; Risperidone - adverse effects ; Risperidone - therapeutic use ; Schizophrenia ; Schizophrenia - drug therapy ; Schizophrenic Psychology ; Thiazoles - adverse effects ; Thiazoles - therapeutic use</subject><ispartof>Psychiatry and clinical neurosciences, 2009-06, Vol.63 (3), p.322-328</ispartof><rights>2009 The Authors. Journal compilation © 2009 Japanese Society of Psychiatry and Neurology</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5277-8257168dab42db561bdacd49885c36df05b817a0d33be89f34381a7d74737d0c3</citedby><cites>FETCH-LOGICAL-c5277-8257168dab42db561bdacd49885c36df05b817a0d33be89f34381a7d74737d0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21526238$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19566763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okugawa, Gaku</creatorcontrib><creatorcontrib>Kato, Masaki</creatorcontrib><creatorcontrib>Wakeno, Masataka</creatorcontrib><creatorcontrib>Koh, Jun</creatorcontrib><creatorcontrib>Morikawa, Masayuki</creatorcontrib><creatorcontrib>Matsumoto, Naoki</creatorcontrib><creatorcontrib>Shinosaki, Kazuhiro</creatorcontrib><creatorcontrib>Yoneda, Hiroshi</creatorcontrib><creatorcontrib>Kishimoto, Toshifumi</creatorcontrib><creatorcontrib>Kinoshita, Toshihiko</creatorcontrib><title>Randomized clinical comparison of perospirone and risperidone in patients with schizophrenia: Kansai Psychiatric Multicenter Study</title><title>Psychiatry and clinical neurosciences</title><addtitle>Psychiatry Clin Neurosci</addtitle><description>Aim: Perospirone is classified as a second‐generation antipsychotic agent for the treatment of schizophrenia. Perospirone binds with high affinity to serotonin 5‐HT2A receptors and dopamine D2 receptors. There are no reports of clinical comparisons of perospirone and risperidone in multicenter studies. To clarify the clinical traits of perospirone in the treatment of schizophrenia, the clinical efficacies and side‐effects of perospirone and risperidone were compared in a randomized clinical multicenter trial.
Methods: Sixty‐six schizophrenia patients were enrolled in the trial. The Positive and Negative Syndrome Scale (PANSS) total, positive, negative and general symptoms scores and Drug‐Induced Extra‐Pyramidal Symptoms Scale (DIEPSS) scores were investigated at 0, 4, 8 and 12 weeks.
Results: Significant reductions in the PANSS total and subscale scores were observed in both the perospirone and risperidone groups, with no significant between‐group differences at 4 and 12 weeks. Risperidone improved the total scores and overall psychopathologic symptom total scores more effectively than perospirone at week 8. There were no significant differences in the DIEPSS scores at 0, 4, 8 and 12 weeks between the perospirone and risperidone groups. The numbers of patients who dropped out did not differ between the perospirone and risperidone groups.
Conclusions: Perospirone was as effective as risperidone against positive and negative symptoms in patients with schizophrenia. Both antipsychotic agents were equally well‐tolerated.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>Antipsychotic Agents - adverse effects</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>antipsychotics</subject><subject>Basal Ganglia Diseases - chemically induced</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Humans</subject><subject>Isoindoles - adverse effects</subject><subject>Isoindoles - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>neuroleptic</subject><subject>Neuropharmacology</subject><subject>perospirone</subject><subject>Pharmacology. Drug treatments</subject><subject>Psychiatric Status Rating Scales - statistics & numerical data</subject><subject>Psycholeptics: tranquillizer, neuroleptic</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychopharmacology</subject><subject>Psychoses</subject><subject>risperidone</subject><subject>Risperidone - adverse effects</subject><subject>Risperidone - therapeutic use</subject><subject>Schizophrenia</subject><subject>Schizophrenia - drug therapy</subject><subject>Schizophrenic Psychology</subject><subject>Thiazoles - adverse effects</subject><subject>Thiazoles - therapeutic use</subject><issn>1323-1316</issn><issn>1440-1819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkEtv1DAQgC0EoqXwF5AvcEvwI7EdJA5oVR6itBUtZ8uxHe2sEifYidrtkV-Ow67KFV88nvnGHn8IYUpKmte7XUmrihRU0aZkhDQloU0ly_sn6PSx8DTHnPGCcipO0IuUdoQQzgV9jk5oUwshBT9Fv3-Y4MYBHrzDtocA1vTYjsNkIqQx4LHDk49jmiCOweMM41zIKXDrGQKezAw-zAnfwbzFyW7hYZy20Qcw7_E3E5IBfJ32OW_mCBZ_X_oZbO7wEd_Mi9u_RM860yf_6rifoZ-fzm83X4qLq89fNx8vClszKQvFakmFcqatmGtrQVtnrKsapWrLhetI3SoqDXGct141Ha-4okY6WUkuHbH8DL093DvF8dfi06wHSNb3vQl-XJJmREjGFcmgOoA2fzxF3-kpwmDiXlOiV_96p1fNetWsV__6r399n1tfH99Y2sG7f41H4Rl4cwRMyqq7aIKF9MgxWjORh8jchwN3B73f__cA-npzuUb8D-Dxo9k</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Okugawa, Gaku</creator><creator>Kato, Masaki</creator><creator>Wakeno, Masataka</creator><creator>Koh, Jun</creator><creator>Morikawa, Masayuki</creator><creator>Matsumoto, Naoki</creator><creator>Shinosaki, Kazuhiro</creator><creator>Yoneda, Hiroshi</creator><creator>Kishimoto, Toshifumi</creator><creator>Kinoshita, Toshihiko</creator><general>Blackwell Publishing Asia</general><general>Wiley-Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>200906</creationdate><title>Randomized clinical comparison of perospirone and risperidone in patients with schizophrenia: Kansai Psychiatric Multicenter Study</title><author>Okugawa, Gaku ; Kato, Masaki ; Wakeno, Masataka ; Koh, Jun ; Morikawa, Masayuki ; Matsumoto, Naoki ; Shinosaki, Kazuhiro ; Yoneda, Hiroshi ; Kishimoto, Toshifumi ; Kinoshita, Toshihiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5277-8257168dab42db561bdacd49885c36df05b817a0d33be89f34381a7d74737d0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>Antipsychotic Agents - adverse effects</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>antipsychotics</topic><topic>Basal Ganglia Diseases - chemically induced</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Humans</topic><topic>Isoindoles - adverse effects</topic><topic>Isoindoles - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>neuroleptic</topic><topic>Neuropharmacology</topic><topic>perospirone</topic><topic>Pharmacology. Drug treatments</topic><topic>Psychiatric Status Rating Scales - statistics & numerical data</topic><topic>Psycholeptics: tranquillizer, neuroleptic</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Psychoses</topic><topic>risperidone</topic><topic>Risperidone - adverse effects</topic><topic>Risperidone - therapeutic use</topic><topic>Schizophrenia</topic><topic>Schizophrenia - drug therapy</topic><topic>Schizophrenic Psychology</topic><topic>Thiazoles - adverse effects</topic><topic>Thiazoles - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okugawa, Gaku</creatorcontrib><creatorcontrib>Kato, Masaki</creatorcontrib><creatorcontrib>Wakeno, Masataka</creatorcontrib><creatorcontrib>Koh, Jun</creatorcontrib><creatorcontrib>Morikawa, Masayuki</creatorcontrib><creatorcontrib>Matsumoto, Naoki</creatorcontrib><creatorcontrib>Shinosaki, Kazuhiro</creatorcontrib><creatorcontrib>Yoneda, Hiroshi</creatorcontrib><creatorcontrib>Kishimoto, Toshifumi</creatorcontrib><creatorcontrib>Kinoshita, Toshihiko</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Psychiatry and clinical neurosciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okugawa, Gaku</au><au>Kato, Masaki</au><au>Wakeno, Masataka</au><au>Koh, Jun</au><au>Morikawa, Masayuki</au><au>Matsumoto, Naoki</au><au>Shinosaki, Kazuhiro</au><au>Yoneda, Hiroshi</au><au>Kishimoto, Toshifumi</au><au>Kinoshita, Toshihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized clinical comparison of perospirone and risperidone in patients with schizophrenia: Kansai Psychiatric Multicenter Study</atitle><jtitle>Psychiatry and clinical neurosciences</jtitle><addtitle>Psychiatry Clin Neurosci</addtitle><date>2009-06</date><risdate>2009</risdate><volume>63</volume><issue>3</issue><spage>322</spage><epage>328</epage><pages>322-328</pages><issn>1323-1316</issn><eissn>1440-1819</eissn><abstract>Aim: Perospirone is classified as a second‐generation antipsychotic agent for the treatment of schizophrenia. Perospirone binds with high affinity to serotonin 5‐HT2A receptors and dopamine D2 receptors. There are no reports of clinical comparisons of perospirone and risperidone in multicenter studies. To clarify the clinical traits of perospirone in the treatment of schizophrenia, the clinical efficacies and side‐effects of perospirone and risperidone were compared in a randomized clinical multicenter trial.
Methods: Sixty‐six schizophrenia patients were enrolled in the trial. The Positive and Negative Syndrome Scale (PANSS) total, positive, negative and general symptoms scores and Drug‐Induced Extra‐Pyramidal Symptoms Scale (DIEPSS) scores were investigated at 0, 4, 8 and 12 weeks.
Results: Significant reductions in the PANSS total and subscale scores were observed in both the perospirone and risperidone groups, with no significant between‐group differences at 4 and 12 weeks. Risperidone improved the total scores and overall psychopathologic symptom total scores more effectively than perospirone at week 8. There were no significant differences in the DIEPSS scores at 0, 4, 8 and 12 weeks between the perospirone and risperidone groups. The numbers of patients who dropped out did not differ between the perospirone and risperidone groups.
Conclusions: Perospirone was as effective as risperidone against positive and negative symptoms in patients with schizophrenia. Both antipsychotic agents were equally well‐tolerated.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>19566763</pmid><doi>10.1111/j.1440-1819.2009.01947.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Adult and adolescent clinical studies Aged Antipsychotic Agents - adverse effects Antipsychotic Agents - therapeutic use antipsychotics Basal Ganglia Diseases - chemically induced Biological and medical sciences Female Humans Isoindoles - adverse effects Isoindoles - therapeutic use Male Medical sciences Middle Aged neuroleptic Neuropharmacology perospirone Pharmacology. Drug treatments Psychiatric Status Rating Scales - statistics & numerical data Psycholeptics: tranquillizer, neuroleptic Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychopharmacology Psychoses risperidone Risperidone - adverse effects Risperidone - therapeutic use Schizophrenia Schizophrenia - drug therapy Schizophrenic Psychology Thiazoles - adverse effects Thiazoles - therapeutic use |
title | Randomized clinical comparison of perospirone and risperidone in patients with schizophrenia: Kansai Psychiatric Multicenter Study |
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