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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06020248
Other study ID # 22-37861
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2023
Est. completion date November 2025

Study information

Verified date September 2023
Source University of California, San Francisco
Contact Suzaynn F Schick, PhD
Phone 415-514-3535
Email suzaynn@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a pilot study of the effects of dermal melanin on dermal uptake and retention of nicotine. The initial hypothesis is that higher levels of dermal melanin will correlate with lower uptake and longer retention of nicotine in the skin and body.


Description:

This is an interventional pharmacokinetic study comparing the uptake and metabolism of nicotine from smoke-exposed clothing in people with low high levels of dermal melanin and people with high levels of dermal melanin. The study will measure nicotine and metabolites of nicotine in the blood during exposure and in urine for 10 days after exposure.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date November 2025
Est. primary completion date November 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Adult nonsmoker - Aged 18-50 - Skin reflectance scores below 150 or above 249 using the Mexameter 18 instrument - Healthy on the basis of medical history - Systolic blood pressure <150 - Diastolic blood pressure <100 - C-reactive protein <3.1 mg/ml - Liver function (AST and ALT) in normal ranges - kidney function (BUN) in normal ranges - LDL<131 - Blood glucose <110 - Not exposed to tobacco SHS. Exclusion Criteria: - Dermal skin reflectance score between 150 and 249, as measured by the Mexameter 18 instrument. - Positive SARS-CoV-2 antibody test - Age 18 < or > 50 - Physician diagnosis of asthma, heart disease, hypertension, thyroid disease, diabetes, renal or liver impairment or glaucoma. - Unstable psychiatric condition (such as current major depression, history of schizophrenia or bipolar disorder) or current use of more than two psychiatric medications - Systolic blood pressure greater than or equal to 150 - Diastolic blood pressure greater than or equal to 100 - Blood glucose greater than or equal to 110 - LDL greater than or equal to130 - Pregnancy or breastfeeding (by urine hCG and/or history) - Alcohol or illicit drug dependence within the past 5 years - BMI > 35 and < 18 - Current illicit drug use (by history or urine test) - More than 1 pack year smoking history - Ever a daily marijuana smoker - Smoked anything within the last 3 months - Unable to hold allergy or other OTC medicines - Occupational exposure to smoke, dusts OR fumes - Concurrent participation in another clinical trial - Unable to communicate in English - No social security number

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Wear clothing that has been exposed to cigarette smoke for 3 hours.
Cotton clothing is exposed to smoke from Marlboro Red (hard pack) cigarettes at 1-1.2 mg/m3 repeatedly, until total exposure equals 3 grams total particulate material. When tested after exposure, the clothing typically contained 59.15 +/- 18 µg nicotine and 42 +/- 24 ng NNK per gram. The mass of the clothing varies by size, but the average combination of pants and shirt contains 32 mgs nicotine and 23 µg NNK.

Locations

Country Name City State
United States Zuckerberg San Francisco General Hospital San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in blood concentrations of nicotine The study will measure concentration of nicotine in the blood before and after the dermal exposure to nicotine. Baseline and 3 hours
Primary Total combined urinary concentrations of the nicotine metabolites cotinine and 3-hydroxycotinine The study will measure urinary metabolites of nicotine in the first void of the day for 10 days after exposure and sum the total mass of metabolites. First void, collected for 10 days
Secondary Urinary concentration of the NNK metabolite NNAL The study will measure urinary metabolites of NNK in the first void of the day for 10 days after exposure and sum the total mass of metabolites. First void, collected for 10 days
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