CClinicalTrials.gg
TerminatedNCT05598125ECIG-8Updated Oct 28, 2022

Study of Vascular Function Before vs After Smoking an E-cigarette as Compared to a Normal Cigarette

An observational study in Endothelial Function, sponsored by GWT-TUD GmbH. Terminated. Open to male participants aged 22 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-10-28.

Sponsored by GWT-TUD GmbH · Observational

Why this study was terminated
due to recruitment reasons the study was prematurely ended
Study type
Observational
Model
Case-crossover
Time perspective
Prospective
Enrollment
64
Ages
22 Years to 35 Years
Sex
Male
01

Study summary

Investigation of the effect of one-time use of an electronic e-cigarette in comparison to smoking a conventional cigarette on in vivo conduit endothelial function in healthy long-term smokers

Read the detailed description

The overall aim of this study is to compare the short-term vascular effects of smoking an e-cigarette versus smoking a conventional tobacco cigarette in vivo and in vitro.

The specific objectives are as follows:

i. To evaluate the effects of e-cigarette and conventional combustible cigarette (CCC) use on microvascular and macrovascular endothelial function and stiffness in healthy smokers.

ii. To assess circulating markers of endothelial function in response to e-cigarette and CCC smoking.

iii. To investigate the vascular effects of e-cigarette and CCC use on a molecular level by exposing endothelial cells with stimulated serum from the intervention study.

Primary Objective and Outcome Parameter:

The primary objective of this investigator initiated trial (IIT) is to evaluate the short-term effect of e-cigarette puffing on conduit artery function in comparison to smoking a CCC in healthy male long-term smokers.

The relative change in brachial artery diameter in response to reactive hyperemia (flow-mediated vasodilation), a validated surrogate marker of conduit endothelial function, will be used as primary endpoint. FMD [%] is defined as (brachial diameter 60 s after cuff deflation [mm] - baseline brachial diameter [mm]) x 100 / baseline brachial diameter [mm].

The primary outcome measure is the absolute difference of FMD after e-cigarette and CCC.

Secondary Objective and Outcome Parameter:

The secondary objectives are to evaluate in vivo endothelial function in other vascular beds, especially in the microcirculation and the systemic circulation, as well as other aspects of vascular function like stiffness of the arterial tree. Endothelial dysfunction, a key event of atherosclerosis development, is characterized by a respective increase or decrease of endothelium-derived molecules and changes in upstream signaling pathways that control the synthesis and bioavailability of these endothelium-derived molecules. Analysis of circulating biomarkers of endothelial function and expression studies of enzymes involved in endothelial activation will help to closely characterize possible effects of e-cigarette exposure on in vivo endothelial function.

Secondary endpoints are:

  • Augmentation index in response to salbutamol (%) as surrogate of global endothelial function in relation to its response to glyceryl trinitrate (%)
  • Augmentation index (%) as marker of pulse wave reflection and stiffness
  • Retinal arterial and venous diameter in response to flicker-light stimulation (%) as surrogate of microvascular endothelial function
  • Central retinal arterial and venous equivalent and arteriolar-to-venular ratio as indicators of generalized arterial narrowing
  • Circulating biomarkers of endothelial function and activation (Endothelin-1; BH4/BH2) Secondary outcome measures are the absolute differences of secondary endpoints between e-cigarette and CCC (refer to section 13.4.2).

Functional in vitro assays and molecular analyses:

  • mRNA and protein expression of endothelial nitric oxide synthase (eNOS), NRF2 target genes HMOX1, NQO1 and adhesion molecules (ICAM1, VCAM1, SELE, CCL2).
  • Primary cultures of human umbilical vein endothelial cells will be stimulated with serum of human subjects (sampled before or after smoking of one cigarette or e-cigarette) and potential of wound healing will be determined.

Tertiary Objective and Outcome Parameter:

The tertiary objective is to assess differences in vascular function between smokers and never smokers. Tertiary endpoints are baseline values of primary and secondary endpoints.

02

Conditions studied

  • Endothelial Function

Keywords

  • arterial wave reflection
  • microvascular function
  • e-cigarette
03

In context

Lead sponsor

GWT-TUD GmbH is the lead sponsor of 39 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
22 Years to 35 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

80 smokers 25 never smokers will be additionally recruited as a control group who will undergo the same measurements and analyses without smoking intervention.

Inclusion criteria

    • Subjects must be males between 22 and 35 years of age, inclusive.

      • Subjects must be able to comprehend, sign and date a written informed consent prior to entering the study.
      • Subjects must be willing and able to comply with the protocol requirements for the duration of the study.
      • Subjects must have experienced one of the following:

        • Smoked for at least the last 4 years and at least 5 cigarettes a day or 1 pack-years,
        • Never having regularly smoked, i.e. \< 20 cigarettes in their lifetime and not in last 5 years.

Exclusion criteria

Exclusion Criteria:

  • Consumption of cigars, other tobacco and nicotine products and light-cigarettes (less than 8 mg ISO tar).

    • Exhaled CO levels \< 10 ppm (smokers) and ≥ 10 ppm (never smokers).
    • Urinary cotinine \< 200 ng/ml for smoker group
    • Treatment for arterial hypertension, or clinic blood pressure ≥140/90 mmHg.
    • Body mass index ≥ 30 kg/m2
    • Ocular diseases, glaucoma.
    • Convulsive disorder/epilepsy or intake of anticonvulsant drugs.
    • Subjects with a clinically significant or unstable medical or surgical condition that would preclude safe and complete study participation, as determined by medical history, physical exams, ECG, abnormal laboratory tests. Such conditions may include hepatic, renal or metabolic diseases, systemic disease, acute infection, current malignancy or recent history (5 years) of malignancy, major psychiatric disorder, history of drug and/or alcohol abuse and allergies that could be detrimental according to the investigator's judgment.
    • Prior participation in a clinical study in last 4 weeks.
    • Intake of drugs with potential impact on the endothelial function resp. autonomic nervous system.
    • Known intolerance against salbutamol, nitroglycerin and/or propylene glycol.
    • Regular intake of vitamins and mineral supplements.
    • Heavy exercisers and trained athletes (> 5 hours physical activity / week).
05

Study design

Observational model
Case-crossover
Time perspective
Prospective
Enrollment
64 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Smoker_1

    Begins with e-cigarette crosses over to conventional cigarette

    Device: electronic cigarette (e-cigarette) · Device: conventional tobacco cigarette

  • Non smoker

    never smoking participants as control group

  • Smoker_2

    Begins with conventional cigarette crosses over to e-cigarette

    Device: electronic cigarette (e-cigarette) · Device: conventional tobacco cigarette

Interventions

  • Deviceelectronic cigarette (e-cigarette)
  • Deviceconventional tobacco cigarette
06

What researchers measure

Primary outcomes

  1. change in conduit artery function related to the smoking pattern

    Conduit artery function is defined as the relative response of brachial artery diameter to reactive hyperemia termed as flow-mediated vasodilation (FMD). The primary outcome measure is the absolute difference of FMD after e-cigarette and conventional cigarette consume

    Time frame: 7 days

Secondary outcomes

  1. Retinal arterial and venous diameter in response to flicker-light stimulation (%) as surrogate of microvascular endothelial function

    Secondary outcome measures are the absolute differences of secondary endpoints between e-cigarette and CCC

    Time frame: 7 days

  2. Change in CRAE (central retinal arteriolar equivalents)

    To assess circulating marker of endothelial function in response to e-cigarette and CCC smoking. Central retinal arteriolar as marker of retinal structural microvascular abnormalities esp. generalized arteriolar narrowing and venular widening CRAE \[µm\]: will be automatically determined

    Time frame: 7 days

  3. Change in CRVE (central retinal venular equivalents)

    To assess circulating marker of endothelial function in response to e-cigarette and CCC smoking. Central retinal venular equivalents as marker of retinal structural microvascular abnormalities esp. generalized arteriolar narrowing and venular widening CRVE \[µm\]: will be automatically determined

    Time frame: 7 days

  4. Change in AVR (arteriolar-to-venular ratio)

    To assess circulating marker of endothelial function in response to e-cigarette and CCC smoking. Arteriolar-to-venular ratio as marker of retinal structural microvascular abnormalities esp. generalized arteriolar narrowing and venular widening AVR: will be automatically determined

    Time frame: 7 days

  5. Change in circulating biomarkers of endothelial function and activation - Endothelin-1

    To assess circulating marker of endothelial function in response to e-cigarette and CCC smoking. Endothelin-1 \[pg/ml\]

    Time frame: 7 days

  6. Change in circulating biomarkers of endothelial function and activation - BH4/BH2

    To assess circulating marker of endothelial function in response to e-cigarette and CCC smoking. BH4/BH2

    Time frame: 7 days

  7. Augmentation index in response to salbutamol (%) as surrogate of global endothelial function in relation to its response to glyceryl trinitrate (%)

    Secondary outcome measures are the absolute differences of secondary endpoints between e-cigarette and CCC

    Time frame: 7 days

  8. Augmentation index (%) as marker of pulse wave reflection and stiffness

    Secondary outcome measures are the absolute differences of secondary endpoints between e-cigarette and CCC

    Time frame: 7 days

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05598125
Lead sponsor
GWT-TUD GmbH
Responsible party
Sponsor
First posted
Oct 28, 2022
Start date
Jan 9, 2017
Primary completion
Jul 30, 2019
Completion
Jul 30, 2019
Last update
Oct 28, 2022

Study contacts

Tjalf Ziemssen, PhD, MD
study director · Zentrum für Klinische Neurowissenschaften, TU-Dresden
Henning Morawietz, PhD
study director · Bereich Gefäßendothel/Mikrozirkulation, TU-Dresden

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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