Clinical Trial

Anti-HLA Antibodies After Bone Regeneration Surgery

Study acronym: Anti-HLA Bone
Completed
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Summary
This study evaluates the occurrence of anti-human leukocyte antigen (anti-HLA) antibodies following bone regeneration procedures performed prior to dental implant therapy. Allogeneic bone grafts are widely used in regenerative oral surgery due to their favorable osteoconductive and osteoinductive properties; however, their use may be associated with the development of anti-HLA antibodies, which could potentially influence graft integration and healing. Twenty generally healthy adult patients requiring bone augmentation procedures before implant therapy will be included in the study. Patients will receive either a xenogeneic or allogeneic bone graft material during the regenerative procedure. Additionally, half of the participants will receive adjunctive low-level laser therapy (LLLT) in the postoperative period. Blood samples will be collected before surgery and during follow-up to assess anti-HLA antibody levels. Radiological evaluation using cone-beam computed tomography (CBCT) will be performed to assess bone regeneration. After a healing period of approximately 3-6 months, bone samples will be collected during implant placement and analyzed histologically. The study aims to determine whether bone graft origin and photobiomodulation therapy influence anti-HLA antibody development and the healing of regenerated bone tissue.
Trial Details
NCT Number NCT07474857
Lead Sponsor Medical Innovation Center Wroclaw
Collaborators: Wroclaw Medical University
Conditions Alveolar Bone Loss, Maxillary Sinus Bone Loss
Enrollment 20 participants
Start Date 2023-07-01
Primary Completion 2024-12-29 (estimated)
Study Completion 2024-12-29 (estimated)
Updated on ClinicalTrials.gov 2026-03-16