None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Single or multiple missing teeth Subjects with good plaque control and showing good compliance Subjects willing to participate in the study
Exclusion criteria
Exclusion criteria: Subjects with systemic illness, osteoporosis, bleeding disorders, immunocompromised state and debilitating disease etc. Insufficient density or height of residual ridge Pregnant and lactating females Subjects with history of smoking or smokeless tobacco Drug or alcohol abuse Occlusal interferences Subjects with history of allergy Radiotherapy or Chemotherapy for malignancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hard Tissue Measures like primary Implant stability and Secondary implant Stability and Marginal Bone Level Implant Survival Timepoint: Primary stability will be measured immediately after implant placement and secondary stability after 3 months of implant placement Marginal Bone Level will be measured immediately and after 3 months of implant placement and at the time of prosthesis and after 6 months Implant survival at 6 months after prosthesis delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Soft Tissue Measures like Probing Depth & Bleeding on Probing Biomarker evaluation osteocalcin if feasible Patient reported outcomeTimepoint: Probing depth & Bleeding on Probing at 2 weeks ,1 month,3 months & 6 months after prosthesis delivery Biomarker evaluation of osteocalcin at 15 days & 1 month after implant placement if feasible Patient reported outcome for pain & comfort immediately after implant placement & for comfort , masticatory function,speech,esthetics & overall satisfaction after prosthesis delivery | — |
Countries
India
Contacts
Banaras Hindu university