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Recruiting NCT07548398

Gummy Smile and Altered Passive Eruption Prevalence

Conditions: Altered Passive Eruption of Teeth

Sponsor: University of Roma La Sapienza

trial.available_in: БГ
Overview
This observational epidemiological study aims to assess the prevalence of gummy smile and altered passive eruption in a young adult population, with a focus on the second sextant. Periodontal and aesthetic parameters, along with patient-reported discomfort, will be analyzed to identify potential correlations and underlying anatomical factors.
Description
The primary aim of this study is to evaluate the prevalence of gummy smile, with particular focus on altered passive eruption, in a young adult population. Additionally, the study seeks to analyze key aesthetic and periodontal parameters in order to better understand their role in the etiology and clinical manifestation of excessive gingival display. Special attention is given to the second sextant, which is most frequently involved in gummy smile, to investigate the local distribution of these alterations and their diagnostic relevance. Furthermore, the study aims to explore the relationship between the extent of gingival exposure and variations in periodontal parameters, while also assessing the level of aesthetic, psychological, and social discomfort perceived by affected individuals. Data analysis will also allow the identification of potential individual anatomical factors, such as the position of the mucogingival junction and clinical crown dimensions, that may be associated with altered passive eruption. This is an observational epidemiological study designed to evaluate periodontal aesthetic parameters in patients attending their first clinical visit. The study will also assess the presence of aesthetic discomfort, investigate possible correlations, and explore the need for treatment related to second sextant conditions. Patients selected according to specific inclusion and exclusion criteria will undergo an operator-patient interview to collect anamnestic and clinical data. documentation.
Who can participate
Inclusion Criteria: Male and female subjects; Age between 18 and 50 years; Periodontally healthy subjects; Patients with no history of orthodontic treatment; Patients without gingival hypertrophy or hyperplasia. Exclusion Criteria: Age \< 18 or \> 50 years; Patients diagnosed with Stage I-IV periodontitis; Patients currently undergoing orthodontic treatment; Patients with severe dental crowding in the second sextant; Patients taking medications associated with gingival hypertrophy or hyperplasia; Patients unwilling to provide informed consent; Patients with fixed or removable prostheses in the second sextant; Patients with a history of surgical procedures in the second sextant; Patients with uncontrolled diabetes or neuropsychiatric disorders; Patients with infectious diseases; Pregnant or breastfeeding women, or those with suspected pregnancy; Patients taking bisphosphonates; Oncologic patients and those undergoing head and neck radiotherapy or receiving chemotherapy; Patients with alcohol or drug abuse.
Interventions
Clinical assessment
OTHER
Locations 1
Italy (1)
Sapienza università di Roma
Roma , RM
Technical details
Status
Recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
50 Years
Healthy volunteers
No
Start date
01.09.2025
Completion date
01.12.2026
Registry ID
NCT07548398
Source
clinicaltrials.gov
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