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. Healthy gingiva 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 and 1st premolar without any orthodontic anomaly.
Exclusion criteria
Exclusion criteria: 1. Patients diagnosed with destructive periodontal disease. 2. A history of periodontal and peri oral surgery in the anterior maxillary region. 3. Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia. 4. Evidence of caries either on the interproximal surface or at cemento-enamel junction. 5. Presence of an artificial crown, proximal/cervical restorations or abrasions on the Central Incisors, Lateral Incisors and Canines and Premolars. 6. Orthodontically treated teeth. 7. Crowding, spacing, gingival recession with maxillary anterior and premolar teeth.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and correlate Nasolabial Angle and Lip Length with Interdental Smile Line and Gingival Smile Line in Periodontally Healthy Patients.Timepoint: 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) To evaluate Nasolabial angle and lip length in periodontally healthy patients. 2) To evaluate ISL in periodontally healthy patients. 3) To evaluate GSL in periodontally healthy patients. 4) To evaluate the amount of midfacial gingiva visible in GSL. 5) To evaluate the amount of interdental papilla visible in ISL. 6) To correlate the nasolabial angle, lip length with ISL and GSL in periodontally healthy patients. Timepoint: 3 months | — |
Countries
India
Contacts
VSPM Dental College and Research Centre