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Electronic Hookah and Endothelial Cell Function

The Effects of Electronic Hookah on Endothelial Cell Function: The Role of Nicotine

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04133376
Enrollment
33
Registered
2019-10-21
Start date
2020-01-16
Completion date
2023-05-29
Last updated
2026-03-12

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

Conditions

Endothelial Dysfunction, Smoking

Brief summary

Electronic nicotine delivery systems (ENDS) are a rapidly growing global epidemic among adolescents and young adults. Unlike other ENDS such as e-cigarettes, e-hookahs are used through traditional water-pipes, allowing the vapor-containing nicotine, propylene glycol, glycerin, and flavorings-to pass through a water-filled basin, potentially altering the vapor, before it is inhaled through the user's mouth. Contributing to e-hookahs popularity is the belief that the flavored smoke is detoxified as it passes through the water-filled basin, rendering e-hookah a safer tobacco alternative. However, an e-hookahs deliver flavored nicotine by creating a vapor of fine particles and volatile organic compounds that could induce vascular toxicity. While e-hookah vaping acutely reduces endothelial function, the specific role of nicotine and the mechanisms by which it may impairs endothelial function remain understudied. The objective of this project is to investigate the specific role of nicotine in mediating the acute effects of e-hookah vaping on endothelial dysfunction.

Interventions

OTHERElectronic hookah vaping with nicotine

Participants will be invited to vape a 30-minute session of e-hookah containing nicotine

OTHERElectronic hookah vaping without nicotine

Participants will be invited to vape a 30-minute session of e-hookah without containing nicotine

Sponsors

University of California, Los Angeles
Lead SponsorOTHER
Tobacco Related Disease Research Program
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* 21-39 years old hookah smokers: smoked hookah \>12x in last 12 months * 21-39 years old e-cigarette users: vaped \>12x in last 12 months * no history of illicit drugs * no evidence of cardiopulmonary disease by history/ physical * no diabetes: fasting blood glucose \<100 mg/dl * BP\<140/90mmHg * resting HR\<100 bpm * BMI\<30kg•m2 * no prescription medication

Exclusion criteria

* exhaled CO\>10 ppm (smoking non-abstinence) * positive pregnancy test * psychiatric illness

Design outcomes

Primary

MeasureTime frameDescription
Carbon monoxide levelsChanges pre- and post- the 30-minute smoking or vaping exposure sessionsExhaled carbon monoxide levels
Flow-Mediated Dilation (FMD)Changes pre- and post- the 30-minute smoking or vaping exposure sessionsUsing ultrasound, FMD of the brachial artery induced by reactive hyperemia, was used to measure endothelium-dependent vasodilator function. Outcome variable reflecting FMD (brachial artery diameter) was recorded for 45 seconds and resumed 30 seconds before cuff deflation and continuously for 2 minutes after deflation to obtain true peak vasodilatory response.
Acetylcholine-stimulated nitric oxide productionChanges pre- and post- the 30-minute smoking or vaping exposure sessionsHuman umbilical vein endothelial cells were cultured with subjects' serum sampled before and after the vaping sessions and acetylcholine-stimulated nitric oxide production was assessed
Basal reactive oxygen species bioactivityChanges pre- and post- the 30-minute smoking or vaping exposure sessionsHuman umbilical vein endothelial cells were cultured with participants' serum sampled before and after the vaping sessions and basal reactive oxygen species bioactivity was assessed
Fibrinogen levelsChanges pre- and post- the 30-minute smoking or vaping exposure sessionsPlasma fibrinogen
Heme oxygenase-1 assayChanges pre- and post- the 30-minute smoking or vaping exposure sessionsHeme oxygenase-1 concentration assay
paraoxonase-1 activityChanges pre- and post- the 30-minute smoking or vaping exposure sessionsparaoxonase-1 activity
HDL protection assayChanges pre- and post- the 30-minute smoking or vaping exposure sessionsHDL protection assay, reflecting the ability of HDL to inhibit oxidation to LDL
Nicotine levelsChanges pre- and post- the 30-minute smoking or vaping exposure sessionsPlasma nicotine

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMary Rezk-Hanna, PhD

University of California, Los Angeles

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026