CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 22 enrolled
Drug / intervention
Amnion Allograft +1 moreother
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/NCT01836783
NCT01836783N/ACompleted

A Prospective Study of Bone Augmentation Techniques in Extraction Sockets

University of Alabama at Birmingham·interventional·Posted Apr 22, 2013·Updated Jun 10, 2024

In Brief

A clinical study evaluating Amnion Allograft and Allograft for Tooth Loss. Completed, enrolled 22 participants across 1 site.

Detailed Summary

The study will compare the density and strength of regenerated bone in extraction sockets after being grafted with two different materials: Bone Allograft and Bone Allograft with Amnion. The investigators hypothesize that sockets grafted with the Amnion graft will exhibit enhanced healing patterns and will accelerate the formation of regenerated bone in the grafted areas.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTooth Loss
CountriesUnited States
CollaboratorsBioDlogics

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 22, 2013
Enrollment StartJan 1, 2013
Primary CompletionJun 1, 2021
Study CompletionOct 1, 2023
TodayJul 2, 2026
Enrollment to primary: 8.4 yearsPosted 13.2 years ago

Interventions

Amnion Allograftother

Atraumatic extraction and grafting procedures will be followed by insertion of a dental implant into the grafted area at week-8. The implant will be restored and be monitored for 24 months post-insertion. Two special dental cone-beam CT images (pre-baseline and week-7) and a minimum of 6 intraoral radiographs will be taken during the study

Allograftother

Atraumatic extraction and grafting procedures will be followed by insertion of a dental implant into to the grafted area at week-8. The implant will be restored and be monitored for 24 months post-insertion. Two special dental cone-beam CT images (pre-baseline and week-7) and a minimum of 6 intraoral radiographs will be taken during the study