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Horizontal Ridge Augmentation With Simultaneous Implant Placement Using Autogenous Ramus Grafts

NCT07209618 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2025-10-07

No results posted yet for this study

Summary

This retrospective observational study evaluated the clinical outcomes of simultaneous implant placement with horizontal ridge augmentation using autogenous mandibular ramus block grafts. Sixteen patients were treated between January 2018 and March 2025. Clinical and radiological data were analyzed to assess implant survival, osseointegration, and graft incorporation.

Conditions

  • Alveolar Bone Loss
  • Tooth Loss / Rehabilitation

Interventions

PROCEDURE

utogenous mandibular ramus block grafting with simultaneous dental implant placement

Horizontal alveolar ridge augmentation performed using autogenous block grafts harvested from the mandibular ramus. The graft was fixed to reconstruct the buccal wall, followed by immediate placement of dental implants in the same surgical session. Prosthetic loading was initiated 4 months postoperatively.

PROCEDURE

Autogenous mandibular ramus block graft with simultaneous implant placement

Horizontal alveolar ridge augmentation performed using autogenous block grafts harvested from the mandibular ramus. The graft was fixed to reconstruct the buccal wall, followed by immediate placement of dental implants in the same surgical session. Prosthetic loading was initiated 4 months postoperatively.

Sponsors & Collaborators

  • Akdeniz University

    lead OTHER

Principal Investigators

  • Ozalp · Akdeniz University

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2025-07-31
Completion
2025-07-31

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT07209618 on ClinicalTrials.gov