Department of Clinical Pharmacy, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.
Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Neurol Sci. 2022 Oct;43(10):6141-6148. doi: 10.1007/s10072-022-06188-4. Epub 2022 Jun 6.
Sleep disturbances are common non-motor symptoms of Parkinson's disease (PD). We aimed to compare the safety and efficacy of trazodone with melatonin and clonazepam in patients with PD and sleep complaints.
This single-center, double-blind, randomized clinical trial was conducted on PD patients with subjective sleep complaints. Eligible patients were randomized 1:1:1 to receive melatonin 3 mg/day, clonazepam 1 mg/day, or trazodone 50 mg/day for 4 weeks. The primary outcome measure was the changes in Pittsburgh Sleep Quality Index (PSQI) scores. The mean change in Epworth Sleepiness Scale (ESS) and RBD screening questionnaire (RBDSQ) was considered as the secondary outcome measures.
A total of 112 eligible patients were randomized and 93 participants, melatonin (n = 31), trazodone (n = 31), and clonazepam (n = 31), completed the study. There was a significant decrease in PSQI scores after 4 weeks of treatment in all groups. The mean changes of PSQI from baseline were similar among the treatment arms (P = 0.325). Mean changes of RBDSQ and ESS from baseline were significantly different between study arms (P < 0.05). Melatonin intake was associated with a higher decrease in RBDSQ score compared to trazodone (P = 0.011) and clonazepam (P = 0.004). Trazodone intake was associated with a higher decrease in ESS score compared to clonazepam (P = 0.010). Mild adverse events were reported in three patients in the clonazepam, two patients in the trazodone group, and none in the melatonin group.
Trazodone 50 mg/day, clonazepam 1 mg/day, and melatonin 3 mg/day were all tolerable and effective in improving sleep quality in patients with PD.
Iranian Registry of Clinical Trials (registration number; IRCT20170821035819N2).
睡眠障碍是帕金森病(PD)常见的非运动症状。我们旨在比较曲唑酮、褪黑素和氯硝西泮治疗 PD 伴睡眠主诉患者的安全性和疗效。
这是一项单中心、双盲、随机临床试验,纳入了有主观睡眠主诉的 PD 患者。符合条件的患者按 1:1:1 随机分为 3 组,分别接受褪黑素 3mg/天、氯硝西泮 1mg/天和曲唑酮 50mg/天,疗程 4 周。主要结局指标为匹兹堡睡眠质量指数(PSQI)评分的变化。次要结局指标为 Epworth 嗜睡量表(ESS)和快速眼动睡眠行为障碍筛查问卷(RBDSQ)的平均变化。
共纳入 112 例符合条件的患者,其中 93 例(褪黑素组 n=31、曲唑酮组 n=31、氯硝西泮组 n=31)完成了研究。所有组在治疗 4 周后 PSQI 评分均显著降低。治疗组间 PSQI 基线至终点的平均变化无显著差异(P=0.325)。组间 RBDSQ 和 ESS 的平均变化差异有统计学意义(P<0.05)。与曲唑酮和氯硝西泮相比,褪黑素组 RBDSQ 评分降低更明显(P=0.011 和 P=0.004)。与氯硝西泮相比,曲唑酮组 ESS 评分降低更明显(P=0.010)。有 3 例患者服用氯硝西泮、2 例患者服用曲唑酮出现轻度不良反应,而服用褪黑素的患者均无不良反应。
曲唑酮 50mg/天、氯硝西泮 1mg/天和褪黑素 3mg/天均可改善 PD 患者的睡眠质量,且均耐受良好。
伊朗临床试验注册中心(注册号:IRCT20170821035819N2)。