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吸入 N-氯代牛磺酸在人体中的耐受性:一项双盲随机 I 期临床研究。

Tolerability of inhaled N-chlorotaurine in humans: a double-blind randomized phase I clinical study.

机构信息

District Hospital Vöcklabruck, Department of Pneumology, Vöcklabruck, Austria.

Public Hospital Natters, Department of Pneumology, Natters, Austria.

出版信息

Ther Adv Respir Dis. 2018 Jan-Dec;12:1753466618778955. doi: 10.1177/1753466618778955.

Abstract

BACKGROUND

N-chlorotaurine (NCT), a long-lived oxidant produced by human leukocytes, can be synthesized chemically and used topically as a well-tolerated antiseptic to different body regions including sensitive ones. The aim of this study was to test the tolerability of inhaled 1% NCT in aqueous solution upon repeated application.

METHODS

The study was performed double-blind and randomized with a parallel test group (1% NCT) and control group (0.9% NaCl as placebo). There were two Austrian centres involved, the hospitals, Natters and Vöcklabruck. Healthy, full age volunteers were included, 12 in each centre. A total of 12 patients were treated with NCT, and 12 with placebo, exactly half of each group from each centre. The single dose was 1.2 ml inhaled over a period of 10 min using an AKITA JET nebulizer. One inhalation was done every day for five consecutive days. The primary criterion of evaluation was the forced expiratory volume in 1 second (FEV). Secondary criteria were subjective sensations, further lung function parameters such as airway resistance, physical examination, and blood analyses (gases, electrolytes, organ function values, pharmacokinetic parameters taurine and methionine, immune parameters).

RESULTS

All included 15 females and 9 males completed the treatment and the control examinations according to the study protocol. FEV (100.83% ± 8.04% for NCT and 92.92% ± 11.35% for controls) remained unchanged and constant during the treatment and in control examinations 1 week and 3 months after the treatment (98.75% ± 7.37% for NCT and 91.17% ± 9.46% for controls, p > 0.082 between time points within each group). The same was true for all other objective parameters. Subjective mild sensations with a higher frequency in the test group were chlorine taste ( p < 0.01) and occasional tickle in the throat ( p = 0.057). Taurine and methionine plasma concentrations did not change within 60 min after inhalation or later on.

CONCLUSIONS

Inhaled NCT is well tolerated as in other applications of different body regions. Side effects are mild, topical and transitory. The study was registered prospectively in the European Clinical Trials Database of the European Medicines Agency. The EudraCT number is 2012-003700-12.

摘要

背景

N-氯牛磺酸(NCT)是一种由人类白细胞产生的长寿命氧化剂,可通过化学合成,并作为一种耐受良好的防腐剂局部应用于不同的身体部位,包括敏感部位。本研究旨在测试重复应用于水溶液中的 1%NCT 的吸入耐受性。

方法

该研究采用双盲、随机平行对照试验组(1%NCT)和对照组(0.9%NaCl 作为安慰剂)进行。有两个奥地利中心参与,分别是纳特斯医院和福克拉布吕克医院。纳入了健康、成年志愿者,每个中心各 12 人。总共有 12 名患者接受了 NCT 治疗,12 名患者接受了安慰剂治疗,每组均有来自每个中心的一半患者。单次剂量为 1.2ml,通过 AKITA JET 雾化器吸入 10 分钟。每天吸入一次,连续 5 天。评估的主要标准是用力呼气量(FEV)。次要标准是主观感觉、进一步的肺功能参数(气道阻力)、体格检查和血液分析(气体、电解质、器官功能值、药代动力学参数牛磺酸和蛋氨酸、免疫参数)。

结果

所有纳入的 15 名女性和 9 名男性均按研究方案完成了治疗和对照检查。FEV(NCT 为 100.83%±8.04%,对照组为 92.92%±11.35%)在治疗期间和治疗后 1 周和 3 个月的对照检查中保持不变且恒定(NCT 为 98.75%±7.37%,对照组为 91.17%±9.46%,每组内各时间点之间的差异无统计学意义(p>0.082)。所有其他客观参数也是如此。在试验组中,味觉(p<0.01)和偶尔喉咙发痒(p=0.057)等轻度感觉更为频繁。牛磺酸和蛋氨酸的血浆浓度在吸入后 60 分钟内或之后没有变化。

结论

吸入 NCT 耐受性良好,如同其他身体部位的应用一样。副作用轻微,局部且短暂。该研究已在欧洲药品管理局的欧洲临床试验数据库中进行了前瞻性注册。EudraCT 编号为 2012-003700-12。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d3b/5985600/b2d664791a57/10.1177_1753466618778955-fig1.jpg

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