Comparing implant placement techniques for dental restoration
Clinical and Radiographic Evaluation of Implant Stability in Healed Maxillary Posterior Sites Comparing Osteotome, Osseodensification and Conventional Drilling Implant Placement Techniques: A Randomized Clinical Trial
This study is testing which of three different ways to place dental implants works best for people with missing teeth in the back of their upper jaw.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 36 (estimated) |
| Ages | 25 Years to 70 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza) |
| Trial ID | NCT06599112 on ClinicalTrials.gov |
What this trial studies
This study evaluates the stability of dental implants placed using three different techniques: conventional drilling, Osseodensification with Densah burs, and Osteotomes. Patients with partially edentulous upper posterior ridges will be randomly assigned to one of the three groups for implant placement. The study will measure implant stability and assess crestal bone loss around temporary restorations over a follow-up period of one year. The implants used will feature advanced designs to enhance stability and integration.
Who should consider this trial
Good fit: Ideal candidates are patients aged 25-70 with missing teeth in the upper posterior area and sufficient bone dimensions for implant placement.
Not a fit: Patients who are pregnant, smokers, or have habits that may compromise implant longevity will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved dental implant stability and reduced bone loss, enhancing patient outcomes in dental restoration.
How similar studies have performed: Other studies have shown promising results with similar implant placement techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with an age range of 25-70 years * Patients with systemic health * Patient with missing teeth in the upper posterior area * Patients with D3 or D4 type of alveolar bone * Healed bony sites with sufficient dimension for implant placement * Vertical height (≥ 10 mm) * Bucco-lingual dimension (≥ 5.5 mm) * Mesio-distal width (≥6.5 mm) * Patients with periodontal health (PD \< 4mm, BOP \< 10%) * Inter-arch space of 7.5 to allow implant restoration * Good oral hygiene * Cooperative patients who accepted the trial follow up period and sign the informed consent Exclusion Criteria: * Pregnant females * Smokers * Patients with habits that may compromise the longevity and affect the result of the implant as alcoholism or parafunctional habits * History of radiotherapy or use of bisphosphonates
Where this trial is running
Giza
- Cairo University — Giza, Egypt (Recruiting)
Study contacts
- Study coordinator: Nadine Yehia Mohamed, Bachelor's degree
- Email: nadine.fayed@dentistry.cu.edu.eg
- Phone: 01019885817
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.