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.Healthy gingiva with a plaque and gingival index score of 0â??1 (Loe & Silness 1963) 3.Patients with well-aligned maxillary central incisors lateral incisors and canines. 4.Patients having good physical health. 5.Patients having completed growth and development.
Exclusion criteria
Exclusion criteria: 1.Patients diagnosed with destructive periodontal disease. 2.A history of surgery in the anterior maxillary area or open contact or crowding observed visually without aid. 3.Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia. 4.Evidence of caries either on the inter proximal surface or at cemento-enamel junction. 5.Presence of an artificial crown proximal or cervical restorations or abrasions on the central incisors lateral incisors and canines. 6.Evidence of incomplete passive eruption. 7.Orthodontically treated areas.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the Gingival zenith position from the Vertically bisected midline axis in central incisor lateral incisor and canine in males and females of different age groups.Timepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate Ginival zenith level of lateral incisors in apico-coronal direction relative to the gingival line joining the tangents of the GZP of the adjacent central incisor and canine.Timepoint: 6 months | — |
Countries
India
Contacts
VSPM Dental College and Research Centre, Nagpur