Clinical Trial

Efficacy and Safety of Additive Manufacturing Personalized Titanium Mesh in Guided Bone Regeneration

Recruiting
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Summary
This goal of this single-blind, simple randomized, positive-controlled prospective study is to evaluate the effects of additive-manufactured personalized titanium mesh and traditional titanium mesh in guided bone regeneration for large alveolar bone defects. The study will assess the short-term and long-term efficacy, safety, and incidence of complications of the additive-manufactured personalized titanium mesh, along with an analysis of risk factors. Participants will be followed up for two years after surgery with free-of-charge clinical and radiographic examinations.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-11-14; most recent amendment 2025-03-10.
Status change: Not Yet Recruiting → Recruiting 2025-03-10
Trial Details
NCT Number NCT06692244
Lead Sponsor Hospital of Stomatology, Sun Yat-Sen University
Collaborators: Southern Medical University, China, Meizhou People's Hospital, Shenzhen Stomatology Hospital, Guangzhou Medical University
Conditions Alveolar Bone Atrophy, Guided Bone Regeneration
Enrollment 142 participants
Start Date 2024-11-30
Primary Completion 2027-12 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2025-03-11