Ridge Augmentation: Particulate v/s Block Graft
NCT02487784 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15
Last updated 2018-01-03
Summary
The primary aims of this study are to compare the clinical and histologic results of bone regeneration with a cancellous block allograft versus MinerOss Cortico cancellous particulate allograft mixed with autogenous bone chips after 4 months of healing. Titanium reinforced hd-PTFE (Cytoplast) membrane GBR will be used to cover the bone grafts.
Specific Aim 1: To compare the baseline to 4 month change in clinical ridge width and height.
Specific Aim 2: To compare the histologic percent of vital and nonvital bone and trabecular space at 4 months.
The primary outcome variable is the change in horizontal ridge width. The secondary outcomes are the change in ridge height and the percent histologic composition of the augmented site.
Conditions
- Alveolar Bone Loss
Interventions
- PROCEDURE
-
Block allograft
A cancellous block allograft plus corticocancellous particulate allograft will be used as the positive control treatment.
- PROCEDURE
-
Particulate allograft + autogenous bone chips
The test arm of this study will include a mix of particulate bone allograft and autogenous bone chips.
Sponsors & Collaborators
-
University of Louisville
lead OTHER
Principal Investigators
-
Henry Greenwell, DMD, MSD · Director of Graduate Periodontics, School of Dentistry, University of Louisville.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2015-08-31
- Primary Completion
- 2016-06-30
- Completion
- 2016-06-30
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