Immediate Dental Implant Loading, Implant Loading, Implant Placement, Surface Treatment, Tooth Loss, UV Dental Implant
Conditions
Keywords
UV-photofunctionalization, Dental implants, Posterior maxilla, Immediate loading, Early loading, Conventional loading, Implant stability, Osseointegration, Peri-implant bone changes, Randomized clinical trial
Brief summary
This randomized clinical trial evaluates different loading protocols for UV-photofunctionalized dental implants in the posterior maxilla. Clinical and radiographic outcomes will be assessed during follow
Detailed description
The study compares immediate, early, and conventional loading of UV-photofunctionalized dental implants placed in the posterior maxilla. Implant stability and peri-implant tissue changes will be evaluated clinically and radiographically
Interventions
PROCEDUREImmediate loading of UV-photofunctionalized dental implants
Immediate loading of UV-photofunctionalized dental implants placed in the posterior maxilla.
PROCEDUREEarly loading of UV-photofunctionalized dental implants
Early loading of UV-photofunctionalized dental implants placed in the posterior maxilla.
PROCEDUREConventional loading of UV-photofunctionalized dental implants
Conventional loading of UV-photofunctionalized dental implants placed in the posterior maxilla
Sponsors
Mansoura University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
* • Patients with missed single tooth or multiple teeth in posterior maxilla * Patients Free from any para-functional habits. * Patient with Adequate inter-arch relation and inter-occlusal space to accommodate the prosthetic restoration. * Patient with good oral hygiene. * Patients Willing to participate in the study's follow-up intervals.
Exclusion criteria
* • Patients with any local or systemic disease that absolutely contraindicate implant placement or surgery. * Pregnancy. * Patients with any pathological lesion or aggressive periodontal disease at the planned surgical site. * Patients on drugs that could affect bone healing process such as bisphosphonate. * Smokers. * Uncooperative patients.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Implant Stability | -Immediately after impant placement -immediately after loading -3 months after loading - 6 months after loading | Implant stability will be evaluated using Osstell device based on resonance frequency analysis (ISQ values). |
| Hard Tissue (peri-implant bone) | - Immediately Postoperative (baseline) - 3 months after loading. - 6 months after loading. | Marginal bone loss will be assessed using CBCT measured in mm. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Soft Tissue | At 6 months after loading. | The peri-implant mucosa will be evaluated for signs of inflammation using the Modified Sulcus Bleeding Index (mSBI). |
| Peri-implant probing depth | At 6 months after loading. | Probing depth will be assessed using a calibrated periodontal probe with light pressure and measured in mm. |
Countries
Egypt
Outcome results
None listed