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

Investigating the Secondhand Effects of Hookah Smoking and Vaping

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04661683
Enrollment
12
Registered
2020-12-10
Start date
2021-06-25
Completion date
2027-04-15
Last updated
2026-04-22

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

Conditions

Hookah Smoking, Secondhand Aerosol, Vaping, Vascular Stiffness

Brief summary

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.

Interventions

OTHERCombustible Hookah Smoke

Exposure to combustible hookah smoke for a duration of 60 minutes.

OTHERElectronic Hookah Aerosol

Exposure to electronic hookah aerosol for a duration of 60 minutes.

OTHERClean Room Air

Exposure to room air for a duration of 60 minutes.

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 49 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Flow-Mediated Dilation (FMD)Pre- and post- the 60-minute exposure sessionsUsing ultrasound, FMD of the brachial artery induced by reactive hyperemia, will be used to measure endothelium-dependent vasodilator function. Baseline diameter and velocity will be recorded for 45 seconds and resumed 30 seconds before cuff deflation and continuously for 2 minutes after deflation to obtain true peak vasodilatory response.
Arterial stiffnessPre- and post- the 60-minute exposure sessionsUsing applanation tonometry, pulse wave velocity will be used to measure cebtral arterial stiffness.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026