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Clinical Trial Summary

This randomized, parallel design, controlled study will assess the histologic healing of this Ossix™ Bone in humans and compare it to a Bio-Oss® Collagen that is well researched. Subjects will be enrolled into 2 groups. Each subject will provide a single non-molar tooth site for study treatment. The tooth will be extracted, the extraction socket will be filled with one of the study bone grafts. No wound dressing or membrane will be used to cover the bone graft material as both materials can be used alone. An core biopsy will be collected after 16 weeks of healing during the implant placement. The study will evaluate if there is a difference in histologic wound healing following tooth extraction and ridge preservation between groups treated with Bio-Oss® Collagen compared to Ossix™ Bone.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04338516
Study type Interventional
Source Datum Dental LTD
Contact
Status Completed
Phase Phase 4
Start date November 1, 2019
Completion date March 10, 2022

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05047861 - Implant Placement in the Preserved Socket Using Socket Shield Technique With Autogenous Dentin Graft Versus Preserved Socket Using Socket Shield With Alloplast N/A