CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 38 enrolled
Drug / intervention
Bio-Oss® +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03769376
NCT03769376N/ACompleted
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Histologic Comparison of Healing After Tooth Extraction With Ridge Preservation Using Two Different Xenografts

University of Colorado, Denver·interventional·Posted Dec 7, 2018·Updated Dec 15, 2021

In Brief

A clinical study evaluating Bio-Oss® and Salvin-Oss® for Partial Edentulism. Completed, enrolled 38 participants across 1 site.

Detailed 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®.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPartial Edentulism
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedDec 7, 2018
Enrollment StartMay 22, 2019
Primary CompletionMar 15, 2021
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 7.6 years ago

Interventions

Bio-Oss®device

Bio-Oss® xenograft bone material will be placed into the socket following tooth extraction.

Salvin-Oss®device

Salvin-Oss® xenograft bone material will be placed into the socket following tooth extraction.