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树舌胃可欣胶囊I期临床耐受性研究
引用本文:王文萍,张锡玮,李晓斌,陈颖萍,李晓,韩可丽.树舌胃可欣胶囊I期临床耐受性研究[J].辽宁中医杂志,2008,35(2):183-184.
作者姓名:王文萍  张锡玮  李晓斌  陈颖萍  李晓  韩可丽
作者单位:辽宁中医药大学附属医院,辽宁,沈阳,110032
摘    要:目的:评价健康志愿者单次及连续口服树舌胃可欣胶囊的安全性和耐受性,推荐临床安全有效的用药剂量。方法:单次给药的耐受性试验:24名健康受试者,按不同性别分别分配到5个剂量组,分别给予树舌胃可欣胶囊0.3、0.6、1.2、2.4、3.9g。多次给药的耐受性试验:12名健康受试者按不同性别分别分配到2.4g/人或3.9g/人组,每日1次,连续给药7d。观察各组用药后的临床症状、生命体征,检查心电图、血尿常规、肝肾功能、凝血功能、腹部彩超等。结果:单次给药组出现3例血红蛋白、3例红细胞压积、4例PT、1例APTT、1例TT、1例心电图的结果异常,结合其他指标,判断无临床意义。多次给药组出现4例红细胞压积、1例PT、2例APTT、1例TT结果异常,结合其他指标,判断无临床意义。结论:中国健康男性或女性志愿者单次口服树舌胃可欣胶囊在0.3~3.9g/次的剂量范围及多次口服2.4g或3.9g/人是安全的。在II期临床试验中,建议口服树舌胃可欣胶囊的临床用药剂量在每人每次0.3~3.9g范围内可以应用。

关 键 词:树舌胃可欣胶囊  Ⅰ期临床试验  安全性  耐受性
文章编号:1000-1719(2008)02-0183-02
收稿时间:2007-12-25
修稿时间:2007年12月25

Phase I Clinical Trail of Shusheweikexin Capsule in Healthy Volunteers
WANG Wen-ping,ZHANG Xi-wei,LI Xiao-bin,CHEN Ying-ping,LI Xiao,HAN Ke-li.Phase I Clinical Trail of Shusheweikexin Capsule in Healthy Volunteers[J].Liaoning Journal of Traditional Chinese Medicine,2008,35(2):183-184.
Authors:WANG Wen-ping  ZHANG Xi-wei  LI Xiao-bin  CHEN Ying-ping  LI Xiao  HAN Ke-li
Abstract:Objective:To assess the safety and tolerance of single-dose and continuous oral of Shusheweikexin Capsule in Chinese volunteers,thus to establish the effective clinical dosage.Methods:Tolerance test of single-dose intravenous drip:twenty-four healthy volunteers were allocation into 5 single-dose groups by different gender(0.3、0.6、1.2、2.4、and 3.9g respectively).Tolerance test of continuous intravenous drip:twelve healthy volunteers were allocation into 2 multiple-dose groups(2.4 or 3.9g respectively) by different gender,qd×7d.Subjective symptoms,objective signs,vital signs including blood pressure,heart rate,respiration were observed,and routine blood tests,routine urinetests,hepatic function,renal function,clotting function,electroca-rdiogram,abdominal CDFI were monitored after medication.Results:The single-dose groups have three cases of hemoglobin,three cases of hematocrit,four cases of PT,one case of APTT,one case of TT,one case of ECG abnormalities results after treatment,in conjunction with other indicators,judgement without clinical significance.The continuous oral groups have four cases of hematocrit,one case of PT,two cases of APTT,one case of TT abnormalities results after treatment,in conjunction with other indicators,judgement without clinical significance.Conclusions oral administration of a single-dose shusheweikexin capsules 0.3~3.9g/dose,and continuous oral of Shusheweikexin Capsule of 2.4 or 3.9/person in China healthy male or female volunteers is safe.In Phase II clinical trials,recommendate the clinical dosage of oral Shusheweikexin capsule for each person is 0.3 to 3.9g.
Keywords:Shusheweikexin Capsule  phase Ⅰclinical trial  safety  drug tolerance
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