Trials / Completed
CompletedNCT07040124
Assessment of Efficacy of Prebent Titanium Mesh Versus Customized Poly-ether Ether Ketone Mesh for Three Dimensional Augmentation in Deficient Maxillary Ridge. a Randomized Controlled Clinical Trial.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- Basma Alsheikh · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
In conclusion, the choice between titanium and PEEK meshes should consider patient-specific factors, clinical requirements, and surgeon expertise. The PEEK mesh, with its patient customized design enabled by CAD/CAM technology, offers significant advantages, including greater gained bone volume and reduced operative time. Its tailored fabrication ensures precise adaptation to the patient's anatomy, effectively maintaining the space required for optimal bone formation. The integration of such advanced technologies in regenerative procedures represents a significant step forward in achieving predictable outcomes and enhancing patient care. However, continued innovation and evaluation are crucial to refine these approaches and expand their applicability in oral rehabilitation
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | ti mesh | prebent titamesh on a 3-d virtually augmented model |
| PROCEDURE | 3d peek mesh | milled 3d peek mesh |
Timeline
- Start date
- 2020-10-01
- Primary completion
- 2025-01-01
- Completion
- 2025-02-01
- First posted
- 2025-06-27
- Last updated
- 2025-06-27
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07040124. Inclusion in this directory is not an endorsement.