CompletedNot Applicable

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

Egypt10 participantsStarted 2024-05-23

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Participants with vertical alveolar ridge atrophy in the posterior mandible who are motivated, cooperative, and have good oral hygiene. * Minimum of 7 mm remaining bone height from the crest of the alveolar ridge to the inferior alveolar canal. * Patients with adequate remaining interarch space Exclusion Criteria: * Prior local radiation therapy. * Soft and hard tissue pathology at the operation site. * Systemic diseases that might affect bone healing and osseointegration (e.g., uncontrolled diabetes).. * smokers who consume 20 or more cigarettes per day. * patients on anti-resorptive drugs (eg: bisphosphonates and denosumab).

What they're measuring

Vertical Bone Gain in mm

Timeframe: 6 months postoperatively

Trial details

NCT IDNCT07054658

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-01-31

View on ClinicalTrials.gov More Posterior Mandible With Deficient Ridge Height trials