None listed
Conditions
Interventions
Intervention1: NIL: NIL
Sponsors
Dr Abhay Kolte
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 20-60 years. 3. Patients with fully erupted well-aligned remaining teeth without any orthodontic anomaly. 4. Patients exhibiting edentulous area with history of extraction at least one year prior to the commencement of the study.
Exclusion criteria
Exclusion criteria: 1. Artificial crowns, fillings, attrition on the teeth present in the oral cavity. 2. Crowding or spacing in the remaining teeth. 3. Congenitally missing tooth or teeth. 4. Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and classify the localized alveolar bone deficiencies according to the Comprehensive classification system for localized alveolar bone deficiencies in treatment planning for dental implants.Timepoint: baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the vertical bone deficiency in an apico-coronal direction from the cementoenamel junction of the adjacent mesial and distal teeth, the horizontal ridge dimensions in a facio-lingual or buccolingual direction at the cementoenamel junction of the adjacent mesial and distal teeth, the combined vertical bone deficiency and horizontal ridge dimensions, the reliability of the proposed classification system with Siebertâ??s classification and correlate the combined vertical bone deficiency and horizontal ridge dimensions at the site of implant placement with the Comprehensive classification system for localized alveolar bone deficiencies.Timepoint: 3 months | — |
Countries
India
Contacts
Public ContactDr Abhay P Kolte
VSPM Dental College and Research Centre nagpur
Outcome results
None listed