About this trial
* Achieving and maintaining long-term osseointegration for dental implants is a key objective in the field of dentistry. The success of osseointegration is influenced by the surface treatment applied to dental implants. Numerous coating techniques have been developed to improve and speed up osseointegration. * The aim of the current study is to assess immediate dental implant stability coated with erythropoietin gel, both clinically and radiographically. * Materials and Methods: We conducted a randomized controlled clinical trial.The sample will include patients demanding immediate implant treatment in the anterior maxilla . Patients will be randomly allocated into the two groups of the study. The group A will be treated with erythropoietin gel coated dental implant immediately after extraction of non restorable teeth in the anterior maxilla . Group B will be treated with non coated dental implant immediately after extraction of non restorable teeth in the anterior maxilla . * The primary outcome variable will be implant stability and the secondary outcome will be crestal marginal bone level and bone density around implants. It will be measured at time of implant placement and reevaluated after 6-months .
Eligibility criteria
This trial accepts healthy volunteersQualifiers
All patients Should have nonrestorable teeth in the anterior maxilla indicated for extraction and seeking implant placement.
Good general periodontal health and maintenance.
Disqualifiers
Heavy smokers who smoke more than ten cigarettes per day
Acute infected socket
Ant socket with wall defect.
Pregnency
Trial design
Parallel
Treatments tested in this trial
Non coated dental implants
Other interventionPatients with fresh extraction sockets in the anterior maxilla will be treated by non coated immediate implant .
Erythropoietin gel coated implants
Other interventionPatients with fresh extraction sockets in the anterior maxilla will be treated by immediate implant coated by erythropoietin gel.
Treatment groups
Trial outcomes
Primary outcomes
Change in implant stability
Implant stability will be assessed by using ( AnyCheck - Implant Stability Tester ) Utilizes physical tapping technique and dumping capacity analysis to measure implant stability with precision
Secondary outcomes
Change in marginal bone level and bone density around implants
To evaluate the amount of marginal bone loss and bone density around osseointegrated implants, all patient will be subjected to Cone beam computed tomography (CBCT) immediate postoperative and after 6 months.
Sponsors and contacts
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