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用于 COVID-19 无症状或轻度症状成人的口腔漱口液与唾液病毒载量:一项随机、安慰剂对照、开放标签临床试验。

Oral mouthwashes for asymptomatic to mildly symptomatic adults with COVID-19 and salivary viral load: a randomized, placebo-controlled, open-label clinical trial.

机构信息

Department of Oral Microbe Control, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Osaka, 565-0871, Osaka, Japan.

Department of Infection Control and Prevention, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Osaka, 565-0871, Osaka, Japan.

出版信息

BMC Oral Health. 2024 Apr 25;24(1):491. doi: 10.1186/s12903-024-04246-1.

Abstract

BACKGROUND

Recent randomized clinical trials suggest that the effect of using cetylpyridinium chloride (CPC) mouthwashes on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral load in COVID-19 patients has been inconsistent. Additionally, no clinical study has investigated the effectiveness of on-demand aqueous chlorine dioxide mouthwash against COVID-19.

METHODS

We performed a randomized, placebo-controlled, open-label clinical trial to assess for any effects of using mouthwash on the salivary SARS-CoV-2 viral load among asymptomatic to mildly symptomatic adult COVID-19-positive patients. Patients were randomized to receive either 20 mL of 0.05% CPC, 10 mL of 0.01% on-demand aqueous chlorine dioxide, or 20 mL of placebo mouthwash (purified water) in a 1:1:1 ratio. The primary endpoint was the cycle threshold (Ct) values employed for SARS-CoV-2 salivary viral load estimation. We used linear mixed-effects models to assess for any effect of the mouthwashes on SARS-CoV-2 salivary viral load.

RESULTS

Of a total of 96 eligible participants enrolled from November 7, 2022, to January 19, 2023, 90 were accepted for the primary analysis. The use of 0.05% CPC mouthwash was not shown to be superior to placebo in change from baseline salivary Ct value at 30 min (difference vs. placebo, 0.640; 95% confidence interval [CI], -1.425 to 2.706; P = 0.543); 2 h (difference vs. placebo, 1.158; 95% CI, -0.797 to 3.112; P = 0.246); 4 h (difference vs. placebo, 1.283; 95% CI, -0.719 to 3.285; P = 0.209); 10 h (difference vs. placebo, 0.304; 95% CI, -1.777 to 2.385; P = 0.775); or 24 h (difference vs. placebo, 0.782; 95% CI, -1.195 to 2.759; P = 0.438). The use of 0.01% on-demand aqueous chlorine dioxide mouthwash was also not shown to be superior to placebo in change from baseline salivary Ct value at 30 min (difference vs. placebo, 0.905; 95% CI, -1.079 to 2.888; P = 0.371); 2 h (difference vs. placebo, 0.709; 95% CI, -1.275 to 2.693; P = 0.483); 4 h (difference vs. placebo, 0.220; 95% CI, -1.787 to 2.226; P = 0.830); 10 h (difference vs. placebo, 0.198; 95% CI, -1.901 to 2.296; P = 0.854); or 24 h (difference vs. placebo, 0.784; 95% CI, -1.236 to 2.804; P = 0.447).

CONCLUSIONS

In asymptomatic to mildly symptomatic adults with COVID-19, compared to placebo, the use of 0.05% CPC and 0.01% on-demand aqueous chlorine dioxide mouthwash did not lead to a significant reduction in SARS-CoV-2 salivary viral load. Future studies of the efficacy of CPC and on-demand aqueous chlorine dioxide mouthwash on the viral viability of SARS-CoV-2 should be conducted using different specimen types and in multiple populations and settings.

摘要

背景

最近的随机临床试验表明,使用氯化十六烷基吡啶(CPC)漱口水对 COVID-19 患者严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)病毒载量的影响一直不一致。此外,没有临床研究调查按需使用二氧化氯水溶液漱口水对 COVID-19 的有效性。

方法

我们进行了一项随机、安慰剂对照、开放性临床试验,以评估无症状至轻度症状的 COVID-19 阳性成年患者使用漱口水对口咽 SARS-CoV-2 病毒载量的影响。患者被随机分配接受 0.05% CPC 20 毫升、0.01%按需使用二氧化氯水溶液 10 毫升或安慰剂(纯净水)20 毫升,比例为 1:1:1。主要终点是用于 SARS-CoV-2 唾液病毒载量估计的循环阈值(Ct)值。我们使用线性混合效应模型评估漱口水对 SARS-CoV-2 唾液病毒载量的影响。

结果

2022 年 11 月 7 日至 2023 年 1 月 19 日期间共纳入 96 名符合条件的参与者,其中 90 名符合主要分析标准。与安慰剂相比,使用 0.05% CPC 漱口水在 30 分钟时(与安慰剂相比,差异为 0.640;95%置信区间,-1.425 至 2.706;P=0.543)、2 小时时(与安慰剂相比,差异为 1.158;95%置信区间,-0.797 至 3.112;P=0.246)、4 小时时(与安慰剂相比,差异为 1.283;95%置信区间,-0.719 至 3.285;P=0.209)、10 小时时(与安慰剂相比,差异为 0.304;95%置信区间,-1.777 至 2.385;P=0.775)和 24 小时时(与安慰剂相比,差异为 0.782;95%置信区间,-1.195 至 2.759;P=0.438),唾液 Ct 值均未显示出优于安慰剂的变化。使用 0.01%按需使用二氧化氯水溶液漱口水在 30 分钟时(与安慰剂相比,差异为 0.905;95%置信区间,-1.079 至 2.888;P=0.371)、2 小时时(与安慰剂相比,差异为 0.709;95%置信区间,-1.275 至 2.693;P=0.483)、4 小时时(与安慰剂相比,差异为 0.220;95%置信区间,-1.787 至 2.226;P=0.830)、10 小时时(与安慰剂相比,差异为 0.198;95%置信区间,-1.901 至 2.296;P=0.854)和 24 小时时(与安慰剂相比,差异为 0.784;95%置信区间,-1.236 至 2.804;P=0.447),唾液 Ct 值也没有显著降低。

结论

在无症状至轻度症状的 COVID-19 成年患者中,与安慰剂相比,使用 0.05% CPC 和 0.01% 按需使用二氧化氯水溶液漱口水并未导致 SARS-CoV-2 口咽病毒载量显著降低。未来应使用不同的标本类型和在多个人群和环境中进行 CPC 和按需使用二氧化氯水溶液漱口水对 SARS-CoV-2 病毒活力的疗效研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58cd/11044332/f4bda21f1cd3/12903_2024_4246_Fig1_HTML.jpg

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