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Not Yet RecruitingNCT06661447

Bone Augmentation Techniques in the Mandible Posterior Region

Comparison of Bone Augmentation Techniques in the Mandibular Posterior Region: A Randomized Clinical Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
78 (estimated)
Sponsor
Universidad de Especialidades Espiritu Santo · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Accepted

Summary

This study will compare three methods to rebuild lost bone in the back part of the lower jaw (posterior mandible) before dental implant placement. Seventy-eight adults will be randomly assigned to receive one of three "cortical shell" techniques using either the patient's own bone (autogenous) or prefabricated bone plates from animal (xenogeneic) or human donors (allogeneic). In all groups, the space inside the shell will be filled with a mixture of small bone chips and bone substitute material. The main outcome is the increase in jawbone width measured on 3D cone-beam CT scans at 6 months after surgery. Additional scans and clinical assessments up to 12 months will evaluate healing, bone stability, and postoperative recovery.

Conditions

Interventions

TypeNameDescription
PROCEDURECortical Shell Bone GraftingSurgical reconstruction of atrophic posterior mandibular ridges using thin cortical plates fixed with titanium microscrews to form a biologic shell. The inner space is filled with a 1:1 mixture of autogenous bone chips and biomaterial. Depending on the study group, the cortical plates are autogenous (from the mandibular ramus), xenogeneic (bovine origin), or allogeneic (human donor).

Timeline

Start date
2026-04-01
Primary completion
2026-11-01
Completion
2027-04-01
First posted
2024-10-28
Last updated
2026-02-20

Locations

1 site across 1 country: Ecuador

Source: ClinicalTrials.gov record NCT06661447. Inclusion in this directory is not an endorsement.