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Effectiveness, safety and tolerability of a complex homeopathic medicinal product in the prevention of recurrent acute upper respiratory tract infections in children : a multicenter, open, comparative, randomized, controlled clinical trial

机译:复杂顺势疗法药物在预防儿童反复急性上呼吸道感染中的有效性,安全性和耐受性:多中心,开放,比较,随机,对照临床试验

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摘要

Background: The present study was initiated to investigate the effectiveness, safety and tolerability of complex homeopathic CalSuli-4-02 tablets on prevention of recurrent acute upper respiratory tract infections (URTIs) in children, in comparison to another complex homeopathic product. Methods: The study was designed as a prospective, multicenter, randomized, open, clinical trial with two parallel treatment groups at four outpatient pediatric clinics in Russia. Children aged <= 6 years with susceptibility to acute URTIs (>= three occasions during the last 6 months) were randomized to receive either CalSuli-4-02 or a comparator homeopathic product (control group) for 3 weeks. Primary outcome was the frequency of acute URTIs after 3 and 6 months post-treatment follow-up. Secondary endpoints were changes in complaints and symptoms (total and individual scores), treatment satisfaction, antibiotic use, safety and tolerability. Results: The intention-to-treat analysis involved 200 children (CalSuli-4-02: N = 99, Control: N = 101). In both treatment groups, the median number of acute URTIs was one for 3 months and two, respectively, for the full 6 months post-treatment (Relative Risk: 0.86 (95 %-CI: 0.72-1.03), p = 0.1099). Seasons had no influence on the outcome. At the end of study, CalSuli-4-02 had overall higher odds of getting lower complaints severity total score (Odds ratio: 1.99 (95 %-CI: 1.31-3.02), p = 0.0012) and showing symptom improvement (Odds ratio: 1.93 (95 %-CI: 1.25-3.00), p = 0.0033). Specifically, the complaint "appetite disorder" and the symptom "child's activities" significantly improved more in the CalSuli-4-02 group (p = 0.0135 and p = 0.0063, respectively). Antibiotic use was decreased in both treatment groups at the study end. Overall assessment for satisfaction with and tolerability of treatment was higher with CalSuli-4-02. A low number of non-serious adverse drug reactions was reported (CalSuli-4-02: N = 4, Control: N = 1). Conclusions: Both complex homeopathic products led to a comparable reduction of URTIs. In the CalSuli-4-02 group, significantly less URTI-related complaints and symptoms and higher treatment satisfaction and tolerability were detected. The observation that the use of antibiotics was reduced upon treatment with the complex homeopathic medications, without the occurrence of complications, is interesting and warrants further investigations on the potential of CalSuli-4-02 as an antibiotic sparing option.
机译:背景:本研究的开始是为了研究与另一种复杂的顺势疗法产品相比,复杂的顺势疗法CalSuli-4-02片对预防儿童复发性急性上呼吸道感染(URTIs)的有效性,安全性和耐受性。方法:该研究被设计为一项前瞻性,多中心,随机,开放的临床试验,在俄罗斯的四个门诊儿科诊所采用两个平行治疗组。年龄小于等于6岁的儿童对急性URTI易感性(过去6个月中有3次)被随机分配接受CalSuli-4-02或比较顺势疗法产品(对照组)3周。主要结局是治疗后3个月和6个月随访后急性URTIs的发生频率。次要终点是主诉和症状(总分和个人分),治疗满意度,抗生素使用,安全性和耐受性的变化。结果:意向性治疗分析涉及200名儿童(CalSuli-4-02:N = 99,对照组:N = 101)。在两个治疗组中,急性URTI的中位数分别为治疗后6个月的3个月和2个月(相对危险度:0.86(95%-CI:0.72-1.03),p = 0.1099)。季节对结果没有影响。在研究结束时,CalSuli-4-02总体上具有较低的投诉严重度总评分的几率更高(几率:1.99(95%-CI:1.31-3.02),p = 0.0012),并且症状改善(几率: 1.93(95%CI:1.25-3.00),p = 0.0033)。具体而言,在CalSuli-4-02组中,“食欲障碍”和症状“儿童活动”的症状明显改善(分别为p = 0.0135和p = 0.0063)。在研究结束时,两个治疗组的抗生素使用均减少。 CalSuli-4-02对治疗的满意度和耐受性的总体评估较高。据报道,非严重的不良药物反应很少(CalSuli-4-02:N = 4,对照:N = 1)。结论:两种复杂的顺势疗法产品均导致URTIs的下降。在CalSuli-4-02组中,检出的URTI相关症状和症状明显减少,并且治疗满意度和耐受性较高。有趣的是,在使用复杂的顺势疗法药物治疗后减少了抗生素的使用,而没有发生并发症,这一发现很有趣,并且有必要进一步研究CalSuli-4-02作为保留抗生素的可能性。

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