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杜秀兰,张宏,傅新利,张之澧,张梅涧,马永祯.雷络酯片治疗类风湿性关节炎的临床研究[J].中国中西医结合杂志,1998,(2):88-91
雷络酯片治疗类风湿性关节炎的临床研究
Clinical Study on Tripterygium Wilfordii Complex Ester Tablet in Treating Rheumatoid Arthritis
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DOI:
中文关键词:  雷络酯片  雷公藤多甙片  类风湿关节炎
英文关键词:Tripterygium Wilfordii Complex Ester Tablet  Tripterygium Wilfordii Polycoside Tablet  rheumatoid arthritis
基金项目:
作者单位
杜秀兰 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
张宏 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
傅新利 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
张之澧 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
张梅涧 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
马永祯 Du Xiulan, Zhang Hong, Fu Xinli, et al (Affiliated Hospital of Shandong Traditional Chinese Medical University, Jinan (250011 
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中文摘要:
      观察雷公藤叶制剂──雷络酯片治疗类风湿性关节炎的疗效和毒副作用。方法:采用前瞻性、多中心、随机双盲对照的方法,共观察类风湿性关节炎277例,治疗组140,口服雷络酯片,每次2片,每天3次;对照组137例,口服雷公藤根制剂──雷公藤多甙片,每次 2片,每天 3次,均 6周为 1个疗程。结果:治疗组愈显率 25. 71%,总有效率为86. 43%;对照组愈显率 26. 28%,总有效率为 83. 94%,两组比较无显著性差异(P>0. 05)。不良反应的发生率治疗组为 20. 00%,对照组为 23. 35%,两组比较无显著性差异(P>0. 05)。结论:雷公藤叶制剂的有效性及安生性均同于根制剂。
英文摘要:
      To observe the curative effect, toxic and side effect of Tripterygium Wilfordii Complex Ester Tablet (TWT, a preparation of Folium Tripterygium wilfordii) in treating rheumatoid arthritis. Methods: Two hundred and seventy seven patients were observed with prospective, multicentric and random double-blind control method. One hundred and forty cases of TWT group were treated with TWT 2 tablets each time, 3 times a day orally, and the other 137 cases treated with Tripterygium Wilfordii Polycoside Tablet (TPT, a preparation of Radix Tripterygium Wilfordii) 2 tablets each time were taken as control, 3 times a day orally. The therapeutic course for both groups was 6 weeks. Results: The markedly controlled rate of the TWT group was 26. 71% and the total effective rate was 86.43%, while those in the control group were 26. 28% and 83. 94% respectively, the difference between the two groups was insignificant (P>0.05). The occurrence of side-effect in the two groups was 20.00% and 23.35% respectively, also showed no significant difference (P>0.05). Conclusion: The Folium Tripterygium Wilfordii preparation is similar in efficacy and security to the Radix Tripterygium Wilfordii preparation.
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