Implant Site Reaction
Conditions
Brief summary
the purpose of this trial is to evaluate the osseointegration properties of nano-hydroxy apatite coated titanium implants in posterior maxilla. 30 patients will be included in this trial divided into two groups, control and intervention. Primary and secondary implant stability will be measured
Interventions
OTHERnano-hydroxy apatite coated titanium implants
titanium implants with surface treatment of nano-hydroxy apatite
OTHERsandblasted large acid itched coated titanium implant
titanium implants with SLA surface treatment
Sponsors
October University for Modern Sciences and Arts
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
Yes
Inclusion criteria
1. Patients with missing at least one maxillary posterior tooth 2. Patients free from any systemic disease 3. Patients who approve to be included in the trial and sign the informed consent 4. Patients with no intra-bony defect. 5. Adults aged 18 years old and above
Exclusion criteria
1. Patients who are allergic to titanium 2. Heavy smoker patient 3. Patients receiving chemotherapy or radiotherapy 4. Patients who refused to be included in the trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Implant stability | immediately post-operative | implant stability will be measured by radiofrequency analysis |
Countries
Egypt
Outcome results
None listed