MedTrace Logo

Evaluation of Allogenic Bone Ring Graft With Simultaneous Implant Placement for Vertical Ridge Augmentation

NCT07054658 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-07-22

No results posted yet for this study

Summary

This clinical trial aimed to evaluate the effectiveness of vertical ridge augmentation using customized allogenic bone ring grafts with simultaneous dental implant placement in the posterior mandible. The procedure is designed to address vertical bone deficiencies without the need for autogenous bone harvesting, thereby reducing patient morbidity and surgical complexity. The study assessed clinical outcomes including bone gain, implant stability, and over a 6-month period and inflammation, infection, pain and neurosensory changes where assessed for 4 weeks.

Conditions

  • Posterior Mandible With Deficient Ridge Height

Interventions

PROCEDURE

Allogenic Bone Ring Graft With Simultaneous Implant Placement

A surgical procedure involving vertical ridge augmentation using an allogenic bone ring combined with simultaneous dental implant placement in the posterior mandible. The technique allows one-stage treatment of vertical bone defects without the need for autogenous bone harvesting.

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Principal Investigators

  • Ibrahim T Hussein · Faculty of Dentistry, Tanta University, Egypt

  • Rafic R Beder · Faculty of Dentistry, Tanta University, Egypt

  • Khaled A Saad · Faculty of Dentistry, Tanta University, Egypt

  • Maram N Breshah · Faculty of Dentistry, Tanta University, Egypt

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-23
Primary Completion
2025-01-31
Completion
2025-02-27

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07054658 on ClinicalTrials.gov