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首页> 外文期刊>Influenza research and treatment. >Efficacy and Safety of CVT-E002, a Proprietary Extract ofPanax quinquefoliusin the Prevention of Respiratory Infections in Influenza-Vaccinated Community-Dwelling Adults: A Multicenter, Randomized, Double-Blind, and Placebo-Controlled Trial
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Efficacy and Safety of CVT-E002, a Proprietary Extract ofPanax quinquefoliusin the Prevention of Respiratory Infections in Influenza-Vaccinated Community-Dwelling Adults: A Multicenter, Randomized, Double-Blind, and Placebo-Controlled Trial

机译:CVT-E002的功效和安全性,西洋参提取物在流感疫苗接种的社区居住的成年人中预防呼吸道感染:多中心,随机,双盲和安慰剂对照试验

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摘要

CVT-E002 (a proprietary extract) was found to be effective in the prevention of upper respiratory infections (URIs) in healthy adults, and institutionalized and community-dwelling seniors. A multicenter, randomized, double-blind, placebo-controlled trial was carried out to determine effects of CVT-E002 in the prevention of URIs in influenza-vaccinated community-dwelling adults. 783 community-dwelling adults were randomized to receive placebo, 400 mg or 800 mg treatment/d (1 : 1 : 1) for 6 months. Primary analysis on the incidence of laboratory-confirmed-clinical URIs (LCCUs), including influenza A and B, was performed on those receiving at least one dose. Secondary analysis was performed on study completers and included incidence, severity, and duration of URIs meeting a Jackson-based criteria and safety of CVT-E002. The incidence of LCCUs in the ITT group was 5.5%, 5.2%, and 4.6% in the placebo, 400 mg and 800 mg groups, respectively (P=0.89). Jackson-confirmed URIs were significantly lower in the treated groups (P<0.04). CVT-E002 supplementation reduced the severity and duration of Jackson-confirmed URIs. The results indicate that CVT-E002 can be safely used by similar groups and may prevent symptoms of URIs; larger sample size is warranted.
机译:发现CVT-E002(专有提取物)可有效预防健康成年人以及机构化和社区居住的老年人的上呼吸道感染(URI)。进行了一项多中心,随机,双盲,安慰剂对照试验,以确定CVT-E002在预防接种流感疫苗的社区居民中预防URI的作用。 783名居住在社区的成年人随机接受安慰剂,400μmg或800μmg治疗/ d(1 :: 1:1)/ d,共6个月。对接受至少一种剂量的人进行了实验室确认的临床URIs(LCCU)(包括甲型和乙型流感)发生率的初步分析。对研究完成者进行了次要分析,包括符合杰克逊标准和CVT-E002安全性的URI的发生率,严重性和持续时间。 ITT组中LCCU的发生率在安慰剂组,400μmg和800μmg组分别为5.5%,5.2%和4.6%(P = 0.89)。在治疗组中,Jackson确认的URI显着降低(P <0.04)。 CVT-E002补充减少了杰克逊确认的URI的严重性和持续时间。结果表明,CVT-E002可以被相似的人群安全使用,并且可以预防URI症状。保证更大的样本量。

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