Periodontal Health Among Cigarette, Electronic Cigarettes, and Narghile Smokers

April 25, 2026 updated by: 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?

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

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.

Study Type

Observational

Enrollment (Estimated)

90

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Homs Governorate
      • Homs, Homs Governorate, Syria, 0000

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Smoker students at Al-Hawash Private University

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Cigarette Smokers
Non-Interventional Study
E-cigarette Smokers
Non-Interventional Study
Narghile Smokers
Non-Interventional Study

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plaque Index (PI)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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)
Time Frame: 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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2025

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

August 1, 2026

Study Registration Dates

First Submitted

April 25, 2026

First Submitted That Met QC Criteria

April 25, 2026

First Posted (Actual)

May 1, 2026

Study Record Updates

Last Update Posted (Actual)

May 1, 2026

Last Update Submitted That Met QC Criteria

April 25, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 15-6-2025

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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