Mexazolam and alprazolam in the treatment of generalised anxiety disorder - A double-blind, randomised clinical trial

被引:3
|
作者
Vaz-Serra, A
Figueira, ML
Bessa-Peixoto, A
Firmino, H
Albuquerque, R
Paz, C
Dolgner, A
Vaz-Silva, M
Almeida, L [4 ]
机构
[1] Univ Coimbra, Hosp, Dept Psychiat, Coimbra, Portugal
[2] Hosp Santa Maria, Fac Med, Dept Psychiat, Lisbon, Portugal
[3] Hosp S Marcos, Dept Psychiat, Braga, Portugal
[4] Labs BIAL, R&D Dept, P-4745457 S Mamede Do Corondao, Portugal
关键词
D O I
10.2165/00044011-200121040-00003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To compare the anxiolytic effects of mexazolam with those of alprazolam in patients with generalised anxiety disorder (GAD). Methods: Multicentre, randomised, double-blind, parallel-group clinical trial in 64 outpatients with GAD (DSM-IV criteria). Patients were assigned to mexazolam 1mg three times daily (n = 32) or alprazolam 0.5mg three times daily (n = 32) during 1 week, followed sequentially by a period of 2 weeks of reducing dosage according to therapeutic response and by 1-week taper and 1-week treatment-free periods. The Hamilton Anxiety Rating Scale (HAM-A), the Clinical Global Impression (CGI), and the Snaith & Zigmund anxiety and depression self-rating scale (SZS) were used to evaluate the patient's clinical status. Results: Both treatment groups showed a statistically significant anxiolytic effect: a decrease of mean HAM-A score of 16.28 with mexazolam (p < 0.0001 vs baseline) and 14.2 with alprazolam (p <less than> 0.0001) and a reduction in CGI-disease severity score of 2.66 (p < 0.0001) with mexazolam and 2.44 with alprazolam (p < 0.0001). Although a higher absolute rate of responders was observed in the mexazolam group, there were no statistically significant differences in the between-group comparisons (80% vs 70% in HAM-A and 96.7% vs 86.7% in CGI evaluations). Five mexazolam and nine alprazolam recipients reported mild adverse events. Conclusion: Both mexazolam and alprazolam showed a significant anxiolytic effect and were well tolerated in the treatment of GAD, making it an effective pharmacotherapeutic alternative in the treatment of GAD.
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页码:257 / 263
页数:7
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