Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Periodontal Health Among Cigarette, Electronic Cigarettes, and Narghile Smokers

31 de agosto de 2026 actualizado por: Al-Hawash Private University

Evaluation of Periodontal Health Among Cigarette, Electronic Cigarettes, and Narghile Smokers Among a Sample of Alhawsh Private University Students

This study compares the different effects of traditional cigarettes, e-cigarettes, and narghile on periodontal health among a sample of Al-Hawash Private University students. The main question it aims to answer is: Are there statistically significant differences in periodontal parameters among different types of smokers?

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Descripción detallada

The emergence of e-cigarettes and the increasing popularity of hookah smoking, alongside traditional cigarette use, have created a complex health landscape, particularly regarding periodontal health. Despite growing global awareness of smoking-related dangers, particularly among young people due to marketing of "safer" alternatives, there is a lack of research directly comparing the effects of these three smoking methods on periodontal tissues.

While research extensively covers the impact of smoking on periodontal tissues, despite the individual studies on each type of smoking, no study has directly compared the effects of cigarettes, e-cigarettes, and hookah on periodontal health in the same population.

Aim: study and compare the different effects of traditional cigarettes, e-cigarettes, and narghile on periodontal health among a sample of students at Al-Hawash Private University.

Tipo de estudio

De observación

Inscripción (Actual)

90

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Homs Governorate
      • Homs, Homs Governorate, Siria, 0000
        • Al-Hawash Private University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra de probabilidad

Población de estudio

Smoker students at Al-Hawash Private University

Descripción

Inclusion Criteria:

  • Cigarette smokers: Individuals who have smoked five or more cigarettes per day for at least one year.
  • E-cigarette smokers: Individuals who have smoked e-cigarettes one or more times per day for at least one year.
  • narghile smokers: Individuals who have used a hookah one or more times per day for at least one year.

Exclusion Criteria:

  • Non-smokers
  • Ages older than 25 years
  • Dual smokers: Individuals who smoke two or more types of tobacco.
  • Individuals with systemic diseases, such as diabetes, heart disease, liver problems, and kidney disease
  • Individuals who reported using antibiotics, steroids, or NSAIDs within the past month
  • Individuals who have received periodontal treatment at least six months ago

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Cigarette Smokers
Estudio no intervencionista
E-cigarette Smokers
Estudio no intervencionista
Narghile Smokers
Estudio no intervencionista

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Plaque Index (PI)
Periodo de tiempo: At enrollment

Plaque Index (PI) The PI was evaluated according to the Silness and Löe (1964) system. This system assesses the plaque thickness at the tooth cervical margin (closest to the gum) and has four scores:

0: no plaque;

  1. a film of plaque adhering to the free gingival margin which is nonvisible and it can be scraped from the tooth surface using a probe;
  2. moderate accumulation of soft deposits within the gingival pocket or between the tooth and the gingival margin;
  3. abundance of soft matter within the gingival pocket and/or on the tooth and the gingival margin. The presence of visible dental plaque was recorded on the four sites (vestibular, lingual, mesial, and distal) of all the teeth, except the third molars. three PI classes (PI%; [0-1[; [1-2[; [2-3]) were arbitrarily defined
At enrollment
Gingival Index (GI)
Periodo de tiempo: At enrollment

The gingival status was evaluated using the method of Löe and Silness (1963). The GI score perfectly evaluates the marginal and inter proximal tissues separately on the basis of the following three criteria (Löe & Silness, 1963):

0: no inflammation, healthy gingiva;

  1. mild inflammation, slight change in color, slight edema, no bleeding on pressure;
  2. moderate inflammation, moderate glazing, red ness, bleeding on pressure;
  3. severe inflammation, marked redness and hypertrophy, ulceration, tendency to spontaneous bleeding.
At enrollment
Probing Pocket Depth (PPD)
Periodo de tiempo: At enrollment
PPD is the distance between the gingival margin and the apical depth of the periodontal probe tip penetration. The depth of the sulci or pockets was probed using a Williams periodontal probe with markings 1, 2, 3, 5,7,8, 9, 10 mm. The clinical measurements were based on the four sites (buccal, mesial, distal, and lingual) of all the teeth, except the third molars (Natto et al., 2005b).
At enrollment
Clinical Attachment Level (CAL)
Periodo de tiempo: At enrollment
Clinical attachment level (CAL) is measured from the cementoenamel junction to the bottom of the sulcus or pocket at the four sites. The mean is then calculated for each patient.
At enrollment
Bleeding On Probing (BOP)
Periodo de tiempo: At enrollment
The bleeding on probing was assessed through gentle probing of the orifice of the gingival crevice .If bleeding occurs within 10 seconds, a positive finding was established and the number of positive sites was recorded and then expressed as the percentage of the number of sites examined.
At enrollment
Tooth Mobility (TM)
Periodo de tiempo: At enrollment

Tooth mobility, was performed by alternatively pressing on the tooth buccal and lingual surfaces using one finger and one metallic instrument Tooth mobility was recorded (Fleszar et al., 1980) as follows:

0: physiologic mobility, firm tooth;

  1. slightly increased mobility;
  2. definite to considerable increase in mobility but no function impairment;
  3. extreme mobility, a loose tooth that would be incomparable in function
At enrollment
Gingival Recession (GR)
Periodo de tiempo: At enrollment
Gingival recession is measured by measuring the distance from the cementoenamel junction to the free gingival margin at the midpoint of the buccal surface.
At enrollment
Furcation Involvement ( FI)
Periodo de tiempo: At enrollment

Furcation involvement, is investigated clinically with a probe and classified according to the Hamp's classification system:

Class 0 = no horizontal loss of periodontal tissue support (apart from the original scoring scale).

Class I ≤3mm horizontal loss of periodontal tissue support. Class II > 3 mm horizontal loss of periodontal tissue support, no through-and-through furcation Class III through-and-through furcation (required to see the tip of the probe at the contralateral furcation opening) and additionally

At enrollment

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de junio de 2025

Finalización primaria (Actual)

31 de agosto de 2026

Finalización del estudio (Actual)

31 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

25 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

25 de abril de 2026

Publicado por primera vez (Actual)

1 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

31 de agosto de 2026

Última verificación

1 de marzo de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • 15-6-2025

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir