情绪稳定剂和/或抗精神病药物治疗双相I型障碍躁狂发作:随机对照试验的研究方案

Kangguang Lin, Ting Li, Kun Chen, Weicong Lu, Jiehua Kong, Gui-yun Xu
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摘要

背景:在临床实践中,快速有效地治疗双相I型患者的躁狂发作非常重要。因此,有必要制定一种有效的联合两种或多种药物的治疗方案,以便在短时间内(1周)迅速缓解症状。在本临床试验方案中,将使用抗精神病药物喹硫平、奥氮平、齐拉西酮以及情绪稳定剂丙戊酸盐、奥卡西平和锂治疗躁狂发作,探讨这两类药物单独或联合使用的疗效和安全性。方法/设计:本试验将在中国广州脑科医院进行。共有120名双相I型患者,表现出躁狂或混合发作,将接受两个阶段的药物治疗。在第一阶段,患者将被随机分配接受口服丙戊酸盐、奥卡西平、锂、喹硫平、奥氮平或齐拉西酮。在第二阶段,将给予联合药物治疗,即每位患者将接受情绪稳定剂和抗精神病药物的联合治疗。治疗时间为6周。主要结果测量将包括青年躁狂症评定量表(YMRS)分数和辍学率的变化。次要结局指标将包括疾病进展和治疗效果(用临床总体印象量表评估)、症状严重程度(用总体评估量表评估)、焦虑和抑郁症状(分别用汉密尔顿焦虑量表和汉密尔顿抑郁量表评估)。讨论:本试验将为常用处方药的比较疗效和有效性提供初步证据,并尝试优化躁狂和混合发作的药理学治疗。试验注册:ClinicalTrials.gov标识符:NCT01893229;注册于2013年7月2日。
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Mood stabilizers and/or antipsychotic drugs for the treatment of manic episodes in bipolar I disorder: study protocol for a randomized controlled trial
Background: In clinical practice, it is important to quickly and effectively treat manic episodes in patients with bipolar I disorder. Therefore, it is necessary to formulate an effective therapeutic protocol combining two or more drugs in order to rapidly alleviate symptoms within a short time frame (1 week). In this clinical trial protocol, the antipsychotics quetiapine, olanzapine and ziprasidone and the mood stabilizers valproate, oxcarbazepine and lithium will be used to treat manic episodes to investigate the efficacy and safety of these two types of drugs when used alone or in combination. Methods/Design: This trial will be performed at Guangzhou Brain Hospital, China. A total of 120 patients with bipolar I disorder, exhibiting manic or mixed episodes, will undergo two phases of medication. In the first phase, patients will be randomly assigned to receive oral valproate, oxcarbazepine, lithium, quetiapine, olanzapine or ziprasidone. In the second phase, combination drug treatment will be given, i.e., each patient will receive a combination of mood stabilizers and antipsychotics. Treatment will be given for a total of 6 weeks. Primary outcome measures will include changes in the Young Mania Rating Scale (YMRS) scores and dropout rates. Secondary outcome measures will include disease progression and the efficacy of treatment as evaluated with the Clinical Global Impression Scale, symptom severity as evaluated with the Global Assessment Scale, and anxiety and depression symptoms as evaluated with the Hamilton Anxiety Scale and the Hamilton Depression Scale, respectively. Discussion: This trial will provide preliminary evidence on the comparative efficacy and effectiveness of the commonly prescribed drugs, with attempts at optimizing pharmacological treatments of manic and mixed episodes. Trial registration: ClinicalTrials.gov identifier: NCT01893229; registered on 2 July 2013.
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