Clinical Trials Directory

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

TypeNameDescription
PROCEDUREti meshprebent titamesh on a 3-d virtually augmented model
PROCEDURE3d peek meshmilled 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.