None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who are willing to participate and sign the informed consent for this clinical trial. 2. Patients in the age group of 18 to 50 years. 3. No congenitally missing teeth. 4. Patients will be divided as: a) Group 1: 30 patients with Dolichofacial facial patterns b) Group 2: 30 patients with Mesiofacial facial patterns c) Group 3: 30 patients with Brachyfacial facial patterns
Exclusion criteria
Exclusion criteria: 1. Systemic conditions associated with periodontal diseases. 2. History of periodontal treatment within the past 6 months. 3. History of patients with Orthognathic surgery 4. Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate influence of palatal masticatory soft tissue thickness and its relation to skeletal profile and palatal depth in patientsTimepoint: At Baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) To evaluate the skeletal profile in patients. 2) To evaluate the palatal masticatory soft tissue thickness in patients. 3) To evaluate the palatal depth in patients. 4) To correlate palatal masticatory soft tissue thickness to skeletal profile & palatal depth in patients. Timepoint: At Baseline | — |
Countries
India
Contacts
VSPM Dental College and Research Centre