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NCT05936775 Clinical Trial

Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant

Implant Site Reaction Clinical Trial

Official title:
Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant Versus Sandblasted Large Thread Acid Etched Implants in Posterior Maxilla. A Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05936775
Other study ID # 2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 22, 2023
Est. completion date April 5, 2024

Study information
Verified date April 2024
Source October University for Modern Sciences and Arts
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date April 5, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 49 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• nano-hydroxy apatite coated titanium implants
titanium implants with surface treatment of nano-hydroxy apatite
• sandblasted large acid itched coated titanium implant
titanium implants with SLA surface treatment

Locations
Country Name City State
Egypt October University for Modern Sciences and Arts faulty of Dentistry Giza

Sponsors (1)
Lead Sponsor Collaborator
October University for Modern Sciences and Arts

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Implant stability implant stability will be measured by radiofrequency analysis immediately post-operative
Primary Implant stability implant stability will be measured by radiofrequency analysis 4 weeks post-operative
Primary Implant stability implant stability will be measured by radiofrequency analysis 6 weeks post-operative
Primary Implant stability implant stability will be measured by radiofrequency analysis 12 weeks post-operative
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