Suspendu

ECIG-8Comparative Investigation of the One-time Use of an Electronic Cigarette (E-cigarette) Versus a Normal Tobacco Cigarette on Vascular Function in Healthy Male Smokers

0 critères remplis à partir de votre profilVoyez en un coup d'œil comment votre profil répond à chaque critère d'éligibilité.
Ce qui est collecté

Collecte de données

Données recueillies dès le début de l'étude - Prospective
Sans prélèvements ADN
Qui peut participer

De 22 à 35 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Cas croisé

Étude centrée sur les variations d'exposition chez un même individu, avec et sans symptômes, pour étudier les effets à court terme.
Observationnel
Date de début : janvier 2017
Voir le détail du protocole

Résumé

Sponsor principalGWT-TUD GmbH
Dernière mise à jour : 28 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 9 janvier 2017

Date à laquelle le premier participant a commencé l'étude.

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.

Titre officielComparative Investigation of the One-time Use of an Electronic Cigarette (E-cigarette) Versus a Normal Tobacco Cigarette on Vascular Function in Healthy Male Smokers
Sponsor principalGWT-TUD GmbH
Dernière mise à jour : 28 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

64 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Cas croisé

Ce type d'étude compare, pour une même personne, ses habitudes ou expositions juste avant un problème de santé, avec celles d'autres moments. L'objectif est d'identifier ce qui a pu déclencher l'événement.


Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Critères

Homme

Le sexe biologique des participants éligibles à s'inscrire.

De 22 à 35 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Critères

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: * 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).

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Objectifs de l'étude

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.
Cette étude n'a pas de données de localisationAjoutez cette étude à vos favoris pour savoir quand les données de localisation seront disponibles.
SuspenduAucun centre d'étude