the Effect of Hyaluronic Acid on a Prefabricated CAD-CAM Bone Blocks for Ridge Augmentation

Tanta University

Status: Completed

Conditions: Atrophy of Edentulous Alveolar Ridge

Treatments: Procedure: prefabricated CAD-CAM allogeneic bone block sterilized hydrated using saline solution; Procedure: prefabricated CAD-CAM allogeneic bone block hydrated using hyaluronic acid

Study type: Interventional

Funder types: Other

Identifiers

NCT06395818

6789 (Other Identifier)

Details and patient eligibility

About

Each patient will receive 2 prefabricated CAD-CAM allogeneic bone blocks sterilized with gamma rays with different rehydration methods.

Side I: prefabricated CAD-CAM allogeneic bone block sterilized with gamma rays hydrated using hyaluronic acid * Side II: prefabricated CAD-CAM allogeneic bone block sterilized with gamma rays hydrated using saline solution Both blocks are fixed with osteosynthesis screws, covered with non resorbable membranes** The membranes will be removed after 6 months, dental implants will be placed and core biopsy will be collected from the site of the implant placement for histologic evaluation

Full description

10 patients will be included in this study with bilateral atrophic posterior mandible for split mouth research

. group I: prefabricated CAD-CAM allogeneic bone block sterilized with gamma rays hydrated using hyaluronic acid group II: prefabricated CAD-CAM allogeneic bone block sterilized with gamma rays hydrated using saline solution under LA mucoperiosteal flap will be elevated to expose the atrophic ridge then the prefabricated CAD-CAM allogenic block either mixed with hyaluronic acid (group I) or saline (group II) will be fixed in its position with titanium miniscrews , The block was coated with a nonporous d-PTFE membrane then closure of flap with nylon second stage: 6 months later exposure of alveolar ridge core biopsy was taken for histological study then insertion of titanium implants.

the aim of the study is to investigate the effect of hyaluronic acid on a prefabricated CAD- CAM bone blocks for ridge augmentation radiographically and histologically.

Enrollment: 10 patients

Sex: All

Ages: 40 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients between 40 to 65 years old.
• Posterior atrophic mandibular ridge indicated for horizontal and vertical ridge augmentation for dental implant placement.
• Good oral hygiene

Exclusion criteria

• Systemic diseases that affect host healing responses.
• Heavy smoking.
• Poor oral hygiene.
• Traumatic occlusion, sever para-functional habits (ex. bruxism, clenching,)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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10 participants in 2 patient groups

prefabricated CAD-CAM allogeneic bone block hydrated using hyaluronic acid

Experimental group

Description:

mucoperiosteal flap will be elevated to expose the atrophic ridge then the prefabricated CAD-CAM allogenic block will be fixed in its position with titanium miniscrews , The block was coated with a nonporous d-PTFE membrane

Treatment:

Procedure: prefabricated CAD-CAM allogeneic bone block hydrated using hyaluronic acid

prefabricated CAD-CAM allogeneic bone block sterilized hydrated using saline solution

Experimental group

Description:

mucoperiosteal flap will be elevated to expose the atrophic ridge then the prefabricated CAD-CAM allogenic block will be fixed in its position with titanium miniscrews ,The block was coated with a nonporous d-PTFE membrane

Treatment:

Procedure: prefabricated CAD-CAM allogeneic bone block sterilized hydrated using saline solution