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The Prevalence of Gingival Pigmentation Among a Sample of Adult Egyptian Population.

Completed
Conditions
Gingival Pigmentation
Registration Number
NCT05453890
Lead Sponsor
Cairo University
Brief Summary

This observational cross-sectional study aims at determining the prevalence of gingival pigmentation among a sample of adult Egyptian patients attending the diagnostic centre at Faculty of Dentistry, Cairo University and identifying its association with other risk factors.

Detailed Description

* Dental patients will be recruited in a consecutive manner from the diagnostic center, Faculty of Dentistry, Cairo University.

* Medical history will be taken and patients with certain diseases as Addison's disease, Albright's syndrome, Hereditary hemorrhagic telangiectasia, and HIV-associated melanosis or under certain drugs as ACTH, Antimalarial drugs, and Chemotherapeutic agent-busulfan that induce gingival pigmentation will be excluded from the study.

* Patients who met the inclusion criteria will be subjected to thorough oral examination and a full questionnaire will be filled for each patient. Before filling the questionnaire, the aim of the study will be explained to the patient and the patient's acceptance to participate in the survey will be received.

* During examining patients, any patient found with suspicious gingival pigmentation, whether the degree of pigmentation, texture, size, or any clinical signs of malignancy, will be referred to the Oral Medicine department for a thorough oral and lymph nodes examination, and biopsy taking if needed. Also, any other suspicious oral lesion noticed will be treated the same way, and a close follow-up for the patient will be done to ensure that the he/she has gone through all possible examination protocols to exclude any possibility of malignancy or abnormal condition that needs intervention.

* During oral examination of included patients, those will be found to have gingival pigmentation will be classified according to the gingival pigmentation index.

* Non-respondent patients or patients refusing to participate will be reported with the cause of their refusal.

* The Questionnaire will be filled through a face-to-face personal interview with the patient using simple, short, easily comprehended questions.

* The Questionnaire will include a section for information about age, gender, occupation, place of birth and current residential area.

* Detailed information about smoking type (cigarette, shisha, Vape, IQOS, or others), Smoking Frequency, Smoking duration (no. of years) will be gathered

* The degree of satisfaction or dissatisfaction with gingival pigmentation, and the willingness to do a surgical or laser procedure to change it will be evaluated by VAS score.

* Conventional oral examination will be held on a dental unit using the light of the unit.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
374
Inclusion Criteria
  • Adult patients whose age is 18 years old and above.
  • Patient consulting in the diagnostic centre, Faculty of Dentistry, Cairo University.
  • Provide informed consent.
Exclusion Criteria
  • Systemic diseases and syndromes known to be associated with oral melanin pigmentation, such as Addison's disease, Albright's syndrome, Hereditary hemorrhagic telangiectasia, and HIV-associated melanosis (Peeran et al 2014).
  • Patients taking certain drugs that predispose to drug-induced melanin pigmentation, such as: ACTH, Antimalarial drugs, and Chemotherapeutic agent-busulfan (Peeran et al 2014).
  • Tattoos of the oral mucosa
  • Patients having problem in opening their mouth or undergoing inter-maxillary fixation where oral examination will not be possible.
  • Patients diagnosed with psychiatric problems.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Prevalence of gingival pigmentationUp to 30 weeks

Gingival Pigmentation Index which classified pigmentation into 4 scores according to the position and extent of the gingival pigments:

* Score 0: Absence of pigmentation

* Score 1: Spots of brown to black color or pigments.

* Score 2: Brown to black patches but not diffuse pigmentation

* Score 3: Diffuse brown to black pigmentation, marginal, and attached

Secondary Outcome Measures
NameTimeMethod
Gender of the participantUp to 30 weeks

Male or female

Current area of residenceUp to 30 weeks

City of residence

Age of the participant associated risk factorsUp to 30 weeks

Age in years

Duration of smokingUp to 30 weeks

In years

Occupation of the participantUp to 30 weeks

Certain occupations may be a possible risk factor

Frequency of smokingUp to 30 weeks

Number of Cigarettes/day, In case of other types: daily, weekly, twice weekly, monthly

Place of birthUp to 30 weeks

City of birth

Type of smokingUp to 30 weeks

Cigarette, shisha, Vape, IQOS,... etc. certain types may be of variable risk factor

Trial Locations

Locations (1)

Cairo University

🇪🇬

Cairo, Egypt

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