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A Clinical Trial to Evaluate the Safety and Effectiveness of MatrixOssTM Bone Graft

Dental Diseases Clinical Trial

Official title:
A Prospective, Randomized, Multi-center, Parallel Controlled Trial Evaluating the Efficacy and Safety of MatrixOssTM Bone Graft in Bone Defect Repair Caused by Tooth Extraction

Clinical Trial Summary

The objective of this clinical trial is to evaluate the efficacy and safety of MatrixOssTM Bone Graft in bone defect repair caused by tooth extraction.

Clinical Trial Description

This is a prospective, randomized, multi-center and parallel controlled clinical trial. It is planned to be carried out in more than 3 (including 3) hospitals with qualifications as a national-level clinical trial institution. Subjects included will be randomly assigned into the experimental group and the control group at a ratio of 1:1. Those in the experimental group will receive MatrixOssTM Bone Graft plus Bio-Gide membrane, and those in the control group will receive Bio-Oss Bone Graft plus Bio-Gide membrane. To evaluate whether the changes in alveolar ridge height from baseline to 24 weeks postoperative in the experimental group is non-inferior to that in the control group, so as to verify the efficacy and safety of MatrixOssTM Bone Graft developed and manufactured by Collagen Matrix, Inc. for bone defect repair caused by tooth extraction. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05371535
Study type Interventional
Source Collagen Matrix
Contact Meenakshi Paliwal
Phone 201-405-1477
Email mpaliwal@collagenmatrix.com
Status Not yet recruiting
Phase N/A
Start date May 30, 2022
Completion date June 30, 2023
View Details
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