Reboxetine Combination Therapy With Fluoxetine in Moderate to Severe Obsessive-Compulsive Disorder: A Placebo-Controlled, Double-Blind, Randomized Trial.

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY
Clinical Neuropharmacology Pub Date : 2023-09-01 Epub Date: 2023-07-18 DOI:10.1097/WNF.0000000000000564
Erfaneh Hajian Tilaki, Alireza Hasanzadeh, Mohammadreza Shalbafan, Hossein Sanjari Moghaddam, Ahmad Shamabadi, Mahsa Boroon, Shahin Akhondzadeh
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引用次数: 0

Abstract

Objectives: Reboxetine is a potent and selective norepinephrine reuptake inhibitor that was effective in combination with citalopram for resistant obsessive-compulsive disorder (OCD). This study aims to assess its effectiveness and tolerability in combination with fluoxetine in treating OCD.

Methods: In this 2-center, placebo-controlled, and double-blind, randomized clinical trial, 76 patients with OCD were assigned into 2 parallel groups to receive fluoxetine (up to 80 mg/d) plus placebo (F + P) or fluoxetine (up to 80 mg/d) plus reboxetine (F + R) (10 mg twice daily) for 10 weeks. Participants were assessed with the Yale-Brown Obsessive Compulsive Scale (Y-BOCS) at baseline and weeks 5 and 10.

Results: A total of 76 patients completed the trial. There was no significant difference between the 2 groups in baseline Y-BOCS scores. General linear model repeated-measures showed significant effects on time × treatment interaction on total Y-BOCS ( F = 6.33, df = 1.42, P = 0.006) and obsession subscale scores ( F = 10.39, df = 1.48, P < 0.001), and insignificance on compulsion subscale scores ( F = 1.86, df = 1.24, P = 0.173). Reboxetine combination therapy demonstrated a higher partial and complete treatment response rate ( P < 0.01) according to the Y-BOCS total scores. There was no significant difference between the 2 groups in the frequency of adverse effects.

Conclusions: Reboxetine combination therapy with fluoxetine can effectively improve symptoms in patients with OCD in a short period of treatment. However, further studies with larger sample sizes and longer follow-up periods are needed to confirm these findings.This trial was registered with the Iranian Registry of Clinical Trials ( www.irct.ir ; No IRCT20090117001556N129).

瑞波西汀联合氟西汀治疗中重度强迫症:一项安慰剂对照、双盲、随机试验。
目的:瑞波汀是一种强效选择性去甲肾上腺素再摄取抑制剂,与西酞普兰联合治疗顽固性强迫症(OCD)有效。本研究旨在评估其与氟西汀联合治疗强迫症的有效性和耐受性,76例强迫症患者被分为两组,接受氟西汀(高达80mg/d)加安慰剂(F+P)或氟西汀(低达80mg/d+瑞波西汀(F+R)(10mg,每日两次)治疗10周。参与者在基线以及第5周和第10周使用Yale-Brown强迫症量表(Y-BOCS)进行评估。结果:共有76名患者完成了试验。两组间基线Y-BOCS评分无显著差异。一般线性模型重复测量显示,时间×治疗交互作用对Y-BOCS总分(F=6.33,df=1.42,P=0.006)和痴迷分量表得分(F=10.39,df=1.48,P<0.001)有显著影响,根据Y-BOCS总分,瑞波西汀联合治疗的部分和完全治疗有效率较高(P<0.01)。两组的不良反应发生频率无显著差异。结论:瑞波汀与氟西汀联合治疗能在短时间内有效改善强迫症患者的症状。然而,需要更大样本量和更长随访期的进一步研究来证实这些发现。该试验在伊朗临床试验注册中心注册(www.irct.ir;编号IRCT20090117001556N129)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Neuropharmacology
Clinical Neuropharmacology 医学-临床神经学
CiteScore
1.20
自引率
10.00%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Clinical Neuropharmacology is a peer-reviewed journal devoted to the pharmacology of the nervous system in its broadest sense. Coverage ranges from such basic aspects as mechanisms of action, structure-activity relationships, and drug metabolism and pharmacokinetics, to practical clinical problems such as drug interactions, drug toxicity, and therapy for specific syndromes and symptoms. The journal publishes original articles and brief reports, invited and submitted reviews, and letters to the editor. A regular feature is the Patient Management Series: in-depth case presentations with clinical questions and answers.
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