An Observational Study in Japan to Investigate Health Outcomes Associated With the Use of Ploom TECH

An Observational Study in Japan to Investigate Health Outcomes Associated With the Use of Ploom TECH - Cross-Sectional Survey in Japan

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000036304

Enrollment

500

Registered

2020-03-26

Start date

2019-04-06

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Product Users and Non-smokers

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -Subjects who sign the study-specific consent form -Ploom TECH user: Subjects who use Ploom TECH exclusively more than three months -Cigarette smoker: Subjects who smoke cigarettes exclusively more than one year -Non-smoker: Subjects who have never used tobacco products and nicotine containing products etc.

Exclusion criteria

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 -Tobacco industry employees -Employed by the Sponsor, CRO or Clinical Site etc.

Design outcomes

Primary

Measure	Time frame
-Biomarkers of exposure to selected smoke constituents and potential harm relative to smoking -Health condition -Health related QOL -Level of cough	—

Countries

Japan

Contacts

Public ContactChikako Sakaguchi

JAPAN TOBACCO INC. Scientific Regulatoly Affairs, Tobacco Business Headquarters

chikako.sakaguchi@jt.com03-5572-4819

Outcome results