Health Condition 1: null- Patients with atrophic edentulous maxilla and mandible willing for Implant supported prosthesis
Conditions
Interventions
Intervention1: Nil: Nil
Control Intervention1: Ridge width will be measure clinically using Caliper and radiographically using CBCT. Implant exposure will be measured using UNC-12 probe: Gain in ridge
Sponsors
Dr Tarun Kumar AB
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male and female subjects within the age group of 18-45 years 2. Subjects with good general health 3. Subjects with good oral hygiene 4. Horizontal ridge defect with bucco-lingual dimension of > 2mm to 5. Edentulous ridges with one to four teeth missing 6. Horizontal ridge deficiency at the level of alveolar crest 7. Site with small to moderate bone defect 8. Site should allow implant insertion with primary stability and optimal prosthetic positioning
Exclusion criteria
Exclusion criteria: 1. Subjects with compromised medical history that would complicate the outcome of the study 2. Subjects who are smokers, alcoholics and tobacco chewers 3. Women who are pregnant or lactating mothers 4. Radiation therapy to head or neck region within 5 years 5. Subjects with high or moderate parafunctional activity 6. Subjects on drug therapy which can affect the outcome of the treatment (Bisphosphonates, anti-platelets and anti-coagulants) 7. Subjects with vertical ridge defects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The gain in ridge width which is the difference between the post-operative and pre-operative bone widthTimepoint: The gain in ridge width which is the difference between the post-operative and pre-operative bone width | — |
Secondary
| Measure | Time frame |
|---|---|
| Implant stability Quotient (ISQ). ISQ uses resonance frequency analysisTimepoint: Implant stability will be measured at the time of implant placement and 6 months post-operatively | — |
Countries
India
Contacts
Public ContactDr Tanya Jaitly
Bapuji Dental College and Hospital
Outcome results
None listed