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A Randomized, Double-Blind, and Placebo-Controlled Trial of Chinese Herbal Medicine in the Treatment of Childhood Constipation

机译:中草药治疗儿童童年便秘的随机,双盲和安慰剂对照试验

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OBJECTIVES: Management of constipation is still challenging in childhood. The pharmacological effect of XiaojiDaozhi Decoction, a prescription of Chinese Herbal Medicine (CHM), has been well described for the treatment of food and Qi stagnation which account for childhood constipation. However, the efficacy and safety of XiaojiDaozhi Decoction in childhood constipation remains unclear. METHODS: A randomized, double-blind, and placebo-controlled trial was conducted to evaluate the efficacy and safety of XiaojiDaozhi Decoction in childhood constipation. Two hundred children were recruited and randomly allocated to the CHM or placebo group to receive their respective interventions. The duration of treatment was 8 weeks, with a 12-week follow-up. Main outcome measures were complete spontaneous bowel movements and satisfaction with bowel function. Safety and adverse effects were evaluated by blood laboratory measurements. RESULTS: At the end of follow-up, the response rates of CHM and placebo were 62% and 31%, respectively (χ ~(2) = 19.315, P & 0.01). At the end of treatment, recurrence was found in 7 cases (10.14%) in CHM and 11 cases (26.19%) in placebo (χ ~(2) = 4.947, P & 0.05). In the main outcome measures, 56 patients (56%) in the CHM group and 25 patients (25%) in the placebo group were satisfied with their bowel movements (χ ~(2) = 19.940, P & 0.05). Increased complete spontaneous bowel movements ≥3 per week from baseline were found in 40 patients (40%) who received CHM and 19 patients (19%) who received placebo (χ ~(2) = 10.602, P & 0.05). No serious adverse effects were found in any of the recruited cases. DISCUSSION: CHM XiaojiDaozhi Decoction is a safe and effective method for the treatment of childhood constipation.
机译:目标:便秘管理仍然在童年中挑战。萧吉枣汤的药理作用,中草药处方(CHM)的处方,对食品和气滞的治疗进行了很好的描述,涉及儿童时期便秘。然而,小鸡牛汤中儿童时期便秘的疗效和安全性仍然尚不清楚。方法:进行随机,双盲和安慰剂对照试验,以评估小吉岛汤中儿童便秘的疗效和安全性。招募了两百个孩子,随机分配给CHM或安慰剂集团,以获得各自的干预措施。治疗持续时间为8周,随访12周。主要结果措施是完全自发的排便和肠功能满意度。通过血液实验室测量评估了安全性和不利影响。结果:在随访结束时,CHM和安慰剂的响应率分别为62%和31%(χ〜(2)= 19.315,P& 0.01)。在治疗结束时,在安慰剂的7例(10.14%)中发现7例(10.14%)(10.19%)(26.19%),安慰剂(χ〜(2)= 4.947,P& 0.05)。在主要的结果措施中,CHM组中的56名患者(56%)和安慰剂组中的25名患者(25%)对其肠道运动感到满意(χ〜(2)= 19.940,P& 0.05)。在接受ChM和19名患者(19%)的40名患者(40%)中发现了从基线获得的完全自发性排便≥3.3患者(χ〜(2)= 10.602,P& 0.05)。任何招募案件都没有发现严重的不利影响。讨论:CHM小吉岛汤是一种安全有效的治疗儿童课程的方法。

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