Smoker healthy volunteers I70.9
Conditions
Interventions
Group 1: e-cigarette with nicotine (24 mg/ml)
Group 2: filter cigarette (nicotine - 0.7 mg)
Group 3: e-cigarette without nicotine
Sponsors
Universitätsklinikum Schleswig-Holstein Campus Lübeck
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: - age over 18 years - active smoking - written consent to the study protocol - female smokers under oral contraceptives (to avoid hormonal/cyclic dependencies)
Exclusion criteria
Exclusion criteria: - non smoking - pregnancy or lactation - drug or alcohol abuse - participation in other clinical trials - lack of compliance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the measurement of the nicotine concentration in the blood ten minutes after the nicotine application and during follow-up after one and two hours as well as the changes in blood pressure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include changes in peripheral and central hemodynamics, arterial stiffness, endothelias dysfunction and inflammatory markers depending on the various nicotine applications for two hours after vaping e.g. smoking. | — |
Countries
Germany
Contacts
Public ContactKlaas F. Franzen
Universitätsklinikum Schleswig-Holstein Campus Lübeck
Outcome results
None listed