Immediate implant.
Conditions
Interventions
Intervention 1: Intervention group: Immediate implant placement + placement of SigmaGraft-InterOss bone graft material made in the USA in the distance between implant and buccal bone. Intervention 2:
Sponsors
Islamic Azad University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients require removal of a maxillary anterior tooth and the possibility of immediate implant placement in the same site presence of buccal bone Gap space greater than 2 mm between implant and buccal bone
Exclusion criteria
Exclusion criteria: periodontal disease presence of systemic or local diseases that may interfere with bone repair Use of drugs that prevent implant placement or interfere with implant osteointegration Pregnancy addiction to Drug and smoking Presence of acute infection at the implant site Patient undergoing radiotherapy Patients with parafunctional habits such as Bruxism or Clenching
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone dimensional Changes. Timepoint: At the beginning of the study and 6 months after the intervention (immediate implant placement). Method of measurement: Cone Beam Computed Tomography Pictures. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes: 1) Implant failure: Any implant that is removed after placement due to mobility, progressive marginal bone resorption, infection, or any mechanical complication (e.g., implant fracture). 2) Prosthesis failure: All prosthesis that fail with the implant or can not be placed due to implant failure or will be replaced for any reason. 3) Biological or prosthetic complications. Timepoint: 6 months after intervention (implant placement). Method of measurement: Clinical examination and Cone Beam Computed Tomography images. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSalar Chaychi Salmasi
Islamic Azad University
Outcome results
None listed