Healthy, Smoking, Cigarette
Conditions
Brief summary
The aim of this study is to validate two new biomarkers in sputum samples. These are PiP3 (phosphoinositolphospat ) and phosphor proteins, representing important proteins within inflammatory situations of the lung.
Detailed description
Within the study, sputum samples will be collected at 3 repetitive occasions in a 3 week interval of the different donors. The objective is to assess for biomarker specificity and reproducibility in the two groups (smokers and non-smokers). The methods for measurement shall be validated by repetitive measurement of the sputum samples, i.e. comparison of multiple measurements of the same sample and comparison of different samples from the same donor.
Interventions
OTHERInduced sputum procedure
induced sputum is a sputum specimen produced for diagnostic tests by aerosol administration of a hypertonic saline solution.
Sponsors
Fraunhofer-Institute of Toxicology and Experimental Medicine
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* • Healthy male and female subjects, aged 25-45 years. Women will be considered for inclusion if they are not pregnant, as confirmed by pregnancy test and not nursing. Females of childbearing potential need to use a highly effective method of contraception during the entire study (vasectomised partner, sexual abstinence - the lifestyle of the female should be such that there is complete abstinence from intercourse from two weeks prior to the first visit until at least 72 hours after the last visit -, implants, injectables, combined oral contraceptives, hormonal IUDs (intrauterine device) or double-barrier methods, i.e. any double combination of IUD, condom with spermicidal gel, diaphragm, sponge, and cervical cap). * Body weight ≥ 50 kg and BMI (body mass index) within the range 19-32 kg/m² * Smokers need to consume at least ten cigarettes per day and need to have at least ten packyear * Non-smokers need to be non-smoking since at least a year with a smoking history of no more than 1 packyear. * FEV1 (forced expiratory volume at one second)≥80% predicted and FEV1/FVC (forced expiratory vital capacity) ≥70%
Exclusion criteria
* • History of an acute infection four weeks prior to the informed consent visit. * Regular intake of medication. * Past or present disease, which as judged by the investigator, may affect the outcome of this study. These diseases include, but are not limited to, cardiovascular disease, malignancy, hepatic disease, renal disease, hematological disease, neurological disease, endocrine disease or pulmonary disease (including but not confined to chronic bronchitis, emphysema, tuberculosis, bronchiectasis or cystic fibrosis). * Participation in another clinical trial 30 days prior to enrollment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Biomarker assessment | up to 3 weeks | concentration of PiP3 and phosphoproteins in sputum samples |
Countries
Germany
Outcome results
None listed