Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to compare the speed of bone healing of the two most commonly used xenografts on the market, Bio-Oss® and Salvin-Oss® using a tooth extraction ridge preservation model in participants scheduled for tooth extraction and subsequent receipt of a dental implant. Researchers hypothesize that there will be additional vital bone at 16-20 weeks with Salvin-Oss®.


Clinical Trial Description

This study focuses on xenografts to preserve alveolar bone after tooth extraction prior to placement of a dental implant. Extraction sites that are not grafted for ridge preservation may lose up to 50 percent of their ridge width the first year after extraction. Xenografts are one of several products on the market used to maintain ridge width after tooth extraction. This study aims to compare the two most commonly used, FDA-approved xenografts on the market, Bio-Oss® and Salvin-Oss, in the preservation of alveolar bone after extraction of non-molar teeth. The primary objective of this study is to histologically evaluate and compare the percentage of new bone formation in healing extraction sockets of non-molar teeth grafted with Bio-Oss® versus Salvin-Oss®. The secondary aim is to observe clinical changes in ridge height and ridge width after grafting with these two materials. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03769376
Study type Interventional
Source University of Colorado, Denver
Contact
Status Completed
Phase N/A
Start date May 22, 2019
Completion date March 15, 2021

See also
  Status Clinical Trial Phase
Completed NCT00713206 - Prospective Study of NanoTite Implants Placed Into Fresh Sinus-Lift Augmentation Sites (VSSL) N/A
Completed NCT03283241 - Zolidd One ExHex Dental Implant Compared to Uncoated One ExHex Dental Implant in Subjects With Partial Edentulism N/A
Completed NCT00728884 - Study of Certain Prevail Implants Used to Treat All Types of Edentulism in the Maxilla and Mandible
Completed NCT01529775 - Randomized Study of Osseotite Certain Tapered Prevails vs. Osseotite Certain Tapered N/A
Completed NCT03934853 - Study to Confirm Accuracy and Safety of the Inliant Surgical Navigation System N/A
Completed NCT01953991 - OHQoL With Removable Partial Dentures; a Pilot Study N/A
Completed NCT02387970 - Immediate or Delayed Provisionalization in Posterior Healed Sites N/A
Completed NCT02158377 - TM vs TSV Implants Loaded Early vs Conventional in Anterior and Posterior Areas N/A
Completed NCT01324778 - Multi Centre Study Comparing OsseoSpeed TX With OsseoSpeed N/A
Terminated NCT02188212 - Nobel Procera Crown Shaded Zirconia and NobelProceraTM Full Contour Crown IPS e.Max CAD N/A
Completed NCT00728754 - A Study of Certain Prevail Implants Used for the Preservation of Crestal Bone in Short Fixed Bridge Cases. N/A
Completed NCT00728962 - A Study of Osseotite Certain Prevail Implants Used to Support Short Fixed Bridges With Immediate Occlusal Loading.
Active, not recruiting NCT03558347 - CF41102 5-year Clinical Evaluation of Conelog® Implant With 7 mm Length N/A
Withdrawn NCT02590861 - Improving Oral Health Function With Implant Supported Partial Dentures N/A
Completed NCT02507661 - Effect of Alveolar Ridge Preservation on Implant Esthetic Outcomes Phase 4
Completed NCT02404649 - Comparing Conventional Dental Implants and Trabecular Metalâ„¢ Dental Implants After Sinus Floor Elevation N/A
Completed NCT02703168 - Long-term Performance of SLActive Implants After Immediate or Early Loading N/A
Completed NCT01529814 - Assessment of Integration Success of an Implant System With a Novel Abutment Attachment Design in Early Loaded Cases N/A
Completed NCT00782171 - Evaluation of Immediate Versus Delayed Loading of Dental Implants With a Modified Surface Phase 4
Enrolling by invitation NCT04140006 - Efficacy of Antiresorptive and Bone Forming Material on Dental Implants Phase 1/Phase 2