A Cross-sectional Observational Study in Japan to Investigate Biological Effect Associated with the Use of Ploom X
Not Applicable
- Conditions
- Tobacco Product Users and Never smokers
- Registration Number
- JPRN-UMIN000049840
- Lead Sponsor
- JAPAN TOBACCO INC.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
Not provided
Exclusion Criteria
- Subjects who have, or who have a history of, any clinically significant cardiovascular, hepatic, renal, hematological, respiratory, endocrine, metabolic, electrolyte imbalance - Subjects who have received any investigational drug within 4 months prior to the study period - Pregnant or lactating women or women who may be pregnant - Subjects who have positive test result of SARS-CoV-2 test at screening - Subjects who are employed in the tobacco industries, CRO or clinical facility etc.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method