Assessment of Customized 3D Zirconium Versus Titanium Mesh for Anterior Maxillary Ridge Augmentation With Delayed Implant Placement
Condition(s) studied
Investigational drug(s) / intervention(s)
titanium mesh with bone graft with delayed implant placement.: titanium mesh with bone graft with delayed implant placement.
zirconium mesh with bone graft with delayed implant placement.: zirconium mesh with bone graft with delayed implant placement.
Study summary
The aim of the present study is to assess the customized 3D zirconium versus titanium mesh for anterior maxillary ridge augmentation with delayed implant placement.
Eligibility
Primary outcome measure(s)
- clinical evaluation — 6 months
The patients will be followed up clinically postoperatively every 48-72 hours for the first week then after 2weeks then one month and then after 3 months then after 6 months for preserving: Presence/absence of mesh instability, flap dehiscence, exposed mesh, bone graft loss outside the flap, hematoma or laceration.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Tanta university | Tanta | Egypt |
More Tanta University trials in Egypt
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06933030 on ClinicalTrials.gov ↗ ← All trials in Egypt