NCT05280769已完成不适用
Effects of an Oral Nicotine Product in Smokeless Tobacco Users
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 31
- 试验地点
- 2
- 主要终点
- Change in Plasma nicotine concentration
研究概览
简要总结
The purpose of this research study is to find out how three different nicotine pouches and participant's own brand of smokeless tobacco affect blood nicotine levels and how participants feel.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy (determined by self-report)
- •Between the ages of 18-55
- •Willing to provide informed consent, attend the lab sessions and abstain from tobacco/nicotine as required
- •Agree to use designated products according to study protocol
- •Smokeless tobacco users and must report using smokeless tobacco daily. Smokeless tobacco users must have a 'positive' cotinine cassette result to verify nicotine use
排除标准
- •The following self-reported current, diagnosed medical condition(s): heart-related conditions (e.g., recent heart attack/stroke, coronary heart disease), severe immune system disorders (e.g., HIV/AIDS, multiple sclerosis), respiratory disorders (e.g., COPD, asthma), kidney diseases, liver diseases (e.g., cirrhosis), or seizures
- •Other self-reported current, diagnosed medical conditions (e.g., diabetes, thyroid disease, Lyme disease) may be excluded after consultation with the PI and medical monitor: any medical condition/medication that may affect participant safety, study outcomes, or biomarker data will be excluded based on these consultations
- •Self-reported current, diagnosed psychiatric conditions, and who are currently under the care of a physician for psychiatric conditions, or who report current psychiatric treatment or psychotropic medication use
- •Not providing answers to questions related to inclusion/exclusion criteria
- •Breast-feeding or pregnant women (pregnancy tested by urinalysis at screening
- •Weigh less than 110 pounds
- •Intend to quit tobacco/nicotine use in the next 30 days
结局指标
主要结局
Change in Plasma nicotine concentration
时间窗: Baseline to the end of the session, approximately 4 hours
Blood will be taken multiple times in each session to assess the extent to which product use changes plasma nicotine levels compared to baseline
次要结局
未报告次要终点
研究者
研究点 (2)
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