Comparison Between Two Different Healing Abutments in Single Posterior Implants
Condition(s) studied
Investigational drug(s) / intervention(s)
Prefabricated healing abutment with scan peg: 12 participants will receive single posterior implants by fully guided implant protocol followed by placement of prefabricated healing abutment with scan peg having convex emergence profile
Customized healing abutment: 12 participants will receive single posterior implants by fully guided implant protocol followed by placement of custom healing abutment having concave emergence profile
Study summary
The aim of this randomized clinical trial is to evaluate the volumetric analysis of peri-implant soft tissues after 3 months of the use of a prefabricated healing abutment with scan peg in comparison to customized healing abutment.
Eligibility
Primary outcome measure(s)
- Measurement of peri-implant soft tissues volume — 3 months
Each participant will undergo volumetric analysis of peri-implant soft tissues after 3 months healing either after using prefabricated healing abutment with scan peg in comparison to customized healing abutment using a 3D meteorology software (GOM inspect). It will be measured in millimeter cube
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Faculty of Dentistry, Alexandria University, Egypt | Alexandria | Egypt |
More Alexandria 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 NCT06682559 on ClinicalTrials.gov ↗ ← All trials in Egypt