None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who are willing to participate and sign the informed consent for this clinical trial. 2. Males and females between the age group of 20-40 years. 3. Periodontally healthy patients as assessed with a Plaque Index (Silness & Loe 1964) and Gingival Index (Loe & Silness 1963) between the score of 0â??1. 4. Patients with fully erupted, well-aligned maxillary Central Incisors, Lateral Incisors, and Canines without orthodontic anomaly
Exclusion criteria
Exclusion criteria: 1. Artificial crowns, fillings, attrition on anterior teeth. 2. Congenitally missing anterior tooth or teeth. 3. Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia. 4. Patients diagnosed with destructive periodontal disease or hypertrophy. 5. Patients with a history of any periodontal treatment in the past six months. 6. Malaligned or Orthodontically treated teeth. 7. Facial asymmetry
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate influence of Facial height, facial width, interpupillary and intercommisural width over the size of buccal corridor on smiling.Timepoint: baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To assess the anterior Facial height and width in the study population. 2. To assess interpupillary width in the study population. 3. To assess intercommisural width on smiling in the study population. 4. To assess the size of buccal corridor on smiling. 5. To evaluate and correlate the Facial height, facial width, interpupillary and intercommisural width and size of buccal corridor.Timepoint: 3months | — |
Countries
India
Contacts
VSPM Dental College and Research Centre, Nagpur