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Key constituent exposure in tobacco product switching

Comparative Study of Exposure Levels to Key Constituents in Short-Term Switching Among Different Tobacco Products

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106485
Enrollment
Unknown
Registered
2025-07-24
Start date
2025-08-16
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

None listed

Interventions

Tobacco-free oral tobacco group:Five days use of tobacco-free oral tobacco
e-cigarette group:5-day use of e-cigarette
Heated tobacco product group:5-day use of heated tobacco product.
Cigarette group:5-day use of cigarette
Oral tobacco group:5-day use of oral tobacco
Smoking cessation group:Quit smoking for five days.

Sponsors

Shanghai Institute for Biomedical and Pharmaceutical Technologies
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 20 and 55 years old; 2.Cigarette consumers; 3.Have not taken smoking cessation products/drugs (such as smoking cessation candies, smoking cessation patches, smoking cessation medications, etc.) in the week before participating in the study; 4.With a body mass index (BMI) (weight (kg)/height (m)²) between 18.5 and 27.9 (men with a weight of not less than 52 kg and women with a weight of not less than 45 kg); 5.Understand the information provided in the research project and can make their own decisions on whether to participate in the study; 6.Those who voluntarily participate in the study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Those suffering from acute/chronic respiratory system diseases; 2.Those with malignant tumors; 3.Those suffering from acute/chronic digestive system diseases; 4.Those with acute/chronic liver/kidney diseases; 5.Those with cardiovascular diseases or diabetes; 6.Those with immune system diseases or allergic diseases; 7.Those with mental illnesses; 8.Women who are menstruating, breastfeeding or pregnant; 9.Those who have participated in other clinical trials in the last three months; 10.Those who cannot or are unwilling to provide the informed consent form; 11.Subjects with poor compliance; 12.Those without legal capacity or with restricted legal capacity; 13.Any other situations that the researcher deems inappropriate for participating in this study.

Design outcomes

Primary

MeasureTime frame
Changes in smoking behavior parameters;Serum/plasma/urine concentrations of the selected biomarkers;

Countries

China

Contacts

Public ContactYan Che

Shanghai Institute for Biomedical and Pharmaceutical Technologies

cheyan2004@163.com+86 21 64771556

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026