At a glance
ClinicalIndex Comparison RecordN/ACompleted· 28 enrolled
Drug / intervention
FDBA (MinerOss®) + Mucograft® seal +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.
Effect of Mucograft® Seal on Post-extraction Ridge Preservation Using Bone Allograft: A Randomized Controlled Clinical Trial and Radiographic Evaluation
In Brief
A clinical study evaluating FDBA (MinerOss®) + Mucograft® seal and FDBA (MinerOss®) + Collagen Sponge (HeliPLUG®) for Tooth Extraction Status Nos. Completed, enrolled 28 participants.
Detailed Summary
The objective of this study is to evaluate clinically and radiographically the effect of Mucograft® seal when used for the ridge preservation procedure in combination with Freeze Dried Bone Allograft (FDBA) at the extraction site in terms of hard and soft tissue remodeling after 4 months healing period.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTooth Extraction Status Nos
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartMay 2015
First PostedMar 2016
Primary CompletionDec 2016
TodayJul 2026
First PostedMar 3, 2016
Enrollment StartMay 1, 2015
Primary CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 10.3 years ago
Interventions
FDBA (MinerOss®) + Mucograft® sealdevice
Collagen matrix membrane for soft-tissue regeneration
FDBA (MinerOss®) + Collagen Sponge (HeliPLUG®)device
Standard of Care