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Secondhand Effects of Hookah (i.e., Waterpipe) Smoke and Aerosol

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Enrolling

Conditions

Secondhand Aerosol
Vascular Stiffness
Vaping
Hookah Smoking

Treatments

Other: Electronic Hookah Aerosol
Other: Combustible Hookah Smoke
Other: Clean Room Air

Study type

Interventional

Funder types

Other

Identifiers

NCT04661683
20-001570

Details and patient eligibility

About

In the United States, secondhand smoke is the third leading preventable cause of death. Flavored hookah (waterpipe) tobacco smoking, a highly social activity common in hookah bars, is a key source of SHS exposure. While smoke-free air laws have decreased exposure to secondhand smoke, the majority of laws do not include hookah smoking. Thus, as a social outlet for youth and young adults, hookah smoke exposure may harm non-smokers, including women of reproductive age or pregnant, hookah bar workers, children, and individuals with heart and lung disease. While more is known on the acute effects of active hookah smoking and the literature is emerging on active e-hookah vaping, little is known about the acute vascular effects of secondhand exposure to hookah smoke and aerosol. The study aims to examine the acute effects of secondhand exposure of hookah smoke and aerosol on endothelial and vascular function. Eligible volunteers will be invited to participate in a total of 3 study visits (2-3 hours each): e-hookah aerosol exposure, charcoal-heated hookah smoke exposure and smoke-free room air. Non-invasive blood pressure and blood flow measurements will be taken before and after the exposure sessions.

Enrollment

12 estimated patients

Sex

All

Ages

21 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 21-49 years old
  • Never a smoker: do not use any tobacco products or nicotine delivery systems, including cigarettes, cigars (traditional and filtered), cigarillos, hookah, smokeless tobacco (i.e., loose snus, moist snuff, dip, spit, or chewing tobacco), pipe tobacco, snus pouches, dissolvable tobacco or vaping.
  • no evidence of cardiopulmonary disease by history/physical
  • blood pressure (BP) < 140/90 mmHg
  • resting heart rate (HR) < 100 bpm
  • BMI >18 or < 30kg•m2
  • no prescription medication
  • No exposure to environmental tobacco smoke for at least one week prior to the study date.

Exclusion criteria

  • exhaled carbon monoxide >6 ppm
  • (+) pregnancy test
  • other conditions deemed unsafe to participate, such as breastfeeding

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

12 participants in 3 patient groups

Exposure to Combustible Hookah Smoke
Experimental group
Description:
Participants will be exposed to combustible hookah smoke. To mitigate the impact of carryover effects, the exposure sessions will be separated by a minimum of 7-days.
Treatment:
Other: Combustible Hookah Smoke
Exposure to Electronic Hookah Aerosol
Experimental group
Description:
Participants will be exposed to electronic hookah aerosol. To mitigate the impact of carryover effects, the exposure sessions will be separated by a minimum of 7-days.
Treatment:
Other: Electronic Hookah Aerosol
Exposure to Clean Air
Experimental group
Description:
Participants will be exposed to Clean Room Air. To mitigate the impact of carryover effects, the exposure sessions will be separated by a minimum of 7-days.
Treatment:
Other: Clean Room Air

Trial contacts and locations

1

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Central trial contact

Maria M Rivas; Mary Rezk-Hanna, PhD

Data sourced from clinicaltrials.gov

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