None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Signed informed consent Systemically healthy subject Who will be able to comply with all the procedures Periodontally healthy patient with probing depth less than or equal to 3mm Healed extraction sites more than 6 weeks and free of infection Presence of single edentulous area in maxilla or mandible with buccal alveolar bone deficiency Dehisence type of defect during implant placement Initial implant Stability Stable and favorable occlusal relationship, natural tooth adjacent to the implant site
Exclusion criteria
Exclusion criteria: smokers and tobacco users Acute oral Diseases Parafunctional habits Traumatic occlusion Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Vertical defect height on facial aspect Timepoint: at the time of surgery and at 6 months during re-entry surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| Defect width, Soft tissue dehiscence, Membrane exposure, Redness, Width of keratinized tissue on facial aspect of adjacent teeth. probing pocket depth of adjacent teeth swelling Timepoint: Defect width will be evaluated at the time of surgery and at 6 months re-entry, Width of keratinized tissue and probing pocket depth will be evaluated at the time of initial examination, surgery, 4th week, 3rd months and 6th months. Soft tissue dehiscence, membrane exposure, redness and swelling will be evaluated at the time of 1st week, 4th weeks, 3rd months and 6th months after initial surgery. | — |
Countries
India
Contacts
Faculty of Dental Sciences, IMS, BHU