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Clinical Trial Summary

To evaluate a novel technique of bone regeneration and simultaneous implant placement in severely damaged sockets.


Clinical Trial Description

Patients requiring a single implant, presenting severe facial bone loss as a result of previous infection, failed socket grafting or trauma, will enter this cross-sectional study. Socket reconstruction and simultaneous implant placement will be performed through periosteal-guided bone regeneration (PGBR). Implant timing: immediate or delayed. Implants will be encased in a customized shield of autogenous cortical bone harvested from an adjacent site. A re-entry surgery will be performed at 12-17-weeks to evaluate bone regeneration. Peri-implant tissues will be assessed following established success criteria. Implants will be evaluated for the presence of Periimplantitis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04827693
Study type Observational
Source Verdugo, Fernando, DDS
Contact
Status Completed
Phase
Start date January 3, 2019
Completion date April 5, 2021

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