Clinical Trials Research Unit, The University of Auckland, Auckland, New Zealand.
Tob Control. 2010 Apr;19(2):98-103. doi: 10.1136/tc.2009.031567.
To measure the short-term effects of an electronic nicotine delivery device ("e cigarette", ENDD) on desire to smoke, withdrawal symptoms, acceptability, pharmacokinetic properties and adverse effects.
Single blind randomised repeated measures cross-over trial of the Ruyan V8 ENDD.
University research centre in Auckland, New Zealand.
40 adult dependent smokers of 10 or more cigarettes per day.
Participants were randomised to use ENDDs containing 16 mg nicotine or 0 mg capsules, Nicorette nicotine inhalator or their usual cigarette on each of four study days 3 days apart, with overnight smoking abstinence before use of each product.
The primary outcome was change in desire to smoke, measured as "area under the curve" on an 11-point visual analogue scale before and at intervals over 1 h of use. Secondary outcomes included withdrawal symptoms, acceptability and adverse events. In nine participants, serum nicotine levels were also measured.
Over 60 min, participants using 16 mg ENDD recorded 0.82 units less desire to smoke than the placebo ENDD (p=0.006). No difference in desire to smoke was found between 16 mg ENDD and inhalator. ENDDs were more pleasant to use than inhalator (p=0.016) and produced less irritation of mouth and throat (p<0.001). On average, the ENDD increased serum nicotine to a peak of 1.3 mg/ml in 19.6 min, the inhalator to 2.1 ng/ml in 32 min and cigarettes to 13.4 ng/ml in 14.3 min.
The 16 mg Ruyan V8 ENDD alleviated desire to smoke after overnight abstinence, was well tolerated and had a pharmacokinetic profile more like the Nicorette inhalator than a tobacco cigarette. Evaluation of the ENDD for longer-term safety, potential for long-term use and efficacy as a cessation aid is needed. Trial registration No.12607000587404, Australia and New Zealand Clinical Trials Register.
测量电子烟(“电子烟”)对吸烟欲望、戒断症状、可接受性、药代动力学特性和不良反应的短期影响。
瑞烟 V8 电子烟单盲随机重复测量交叉试验。
新西兰奥克兰大学研究中心。
40 名每天吸烟 10 支或以上的成年吸烟者。
参与者随机使用含有 16 毫克尼古丁或 0 毫克胶囊的电子烟、Nicorette 尼古丁吸入器或他们平时的香烟,每个产品在 3 天内每天使用一次,每次使用前有一夜的吸烟戒断。
主要结果是吸烟欲望的变化,用 11 点视觉模拟量表的“曲线下面积”在使用前和使用后 1 小时的间隔内进行测量。次要结果包括戒断症状、可接受性和不良反应。在 9 名参与者中,还测量了血清尼古丁水平。
在 60 分钟内,使用 16 毫克电子烟的参与者比安慰剂电子烟记录的吸烟欲望少 0.82 个单位(p=0.006)。16 毫克电子烟与吸入器之间的吸烟欲望无差异。电子烟比吸入器更舒适(p=0.016),且对口腔和喉咙的刺激更小(p<0.001)。平均而言,电子烟在 19.6 分钟内将血清尼古丁峰值提高到 1.3 毫克/毫升,吸入器在 32 分钟内提高到 2.1 纳克/毫升,香烟在 14.3 分钟内提高到 13.4 纳克/毫升。
经过一夜的戒断,16 毫克瑞烟 V8 电子烟减轻了吸烟欲望,耐受性良好,其药代动力学特征与尼科莱特吸入器更相似,而不是与香烟相似。需要评估电子烟的长期安全性、长期使用的潜力以及作为戒烟辅助工具的疗效。试验注册号:12607000587404,澳大利亚和新西兰临床试验注册中心。