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一项关于利培酮联合莫达非尼治疗慢性精神分裂症的安慰剂对照研究。

A placebo-controlled study of the modafinil added to risperidone in chronic schizophrenia.

机构信息

Psychiatric Research Center, Roozbeh Psychiatric Hospital, Tehran University of Medical Sciences, South Kargar Street, Tehran, 13337, Iran.

出版信息

Psychopharmacology (Berl). 2012 Apr;220(3):591-8. doi: 10.1007/s00213-011-2513-z. Epub 2011 Sep 24.

Abstract

RATIONAL

In recent years, evidence suggests that modafinil may be useful for certain symptom domains of schizophrenia, especially for the negative and cognitive symptoms. However, the results are not consistent.

OBJECTIVE

This study was designed to investigate the effect of modafinil added to risperidone in patients with chronic schizophrenia in a double blind and randomized clinical trial.

METHODS

Participants were inpatients males (35) and females (11), ages 20-49 years at two teaching psychiatric hospital in Iran. All patients were in the active phase of the illness and met DSM-IV-TR criteria for schizophrenia. Patients were allocated in a random fashion 23 patients to risperidone 6 mg/day plus modafinil 200 mg/day and 23 patients to risperidone 6 mg/day plus placebo. The principal measure of outcome was the positive and negative syndrome scale (PANSS). Patients were assessed by a psychiatrist at baseline and after 2, 4, 6 and 8 weeks after the start of medication.

RESULTS

The modafinil group had significantly greater improvement in the negative symptoms as well as PANSS total scores over the 8-week trial. Therapy with 200 mg/day of modafinil was well tolerated and no clinically important side effects were observed.

CONCLUSION

The present study indicates modafinil as a potential adjunctive treatment strategy for treatment of schizophrenia particularly the negative symptoms. Nevertheless, results of larger-controlled trials are needed before recommendation for broad clinical application can be made.

摘要

目的

本研究旨在通过双盲随机临床试验,调查在利培酮基础上加用莫达非尼治疗慢性精神分裂症患者的效果。

方法

参与者为伊朗两家教学精神病院的住院男性(35 例)和女性(11 例),年龄 20-49 岁。所有患者均处于疾病活跃期,符合 DSM-IV-TR 精神分裂症标准。患者以随机方式分为两组,23 例患者接受利培酮 6mg/天加莫达非尼 200mg/天治疗,23 例患者接受利培酮 6mg/天加安慰剂治疗。主要疗效指标为阳性和阴性症状量表(PANSS)。在基线和开始药物治疗后 2、4、6 和 8 周时,由精神科医生对患者进行评估。

结果

在 8 周的试验中,莫达非尼组的阴性症状和 PANSS 总分改善更为显著。每天 200mg 的莫达非尼治疗耐受性良好,未观察到临床重要的不良反应。

结论

本研究表明,莫达非尼可能是治疗精神分裂症,特别是阴性症状的一种潜在辅助治疗策略。然而,在推荐广泛临床应用之前,还需要进行更大规模的对照试验。

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