Clinical Trials Directory

Trials / Completed

CompletedNCT01901783

Ridge Augmentation Without Primary Closure

Ridge Augmentation Comparing the Clinical and Histologic Healing of a Cancellous Block Allograft Plus a Barrier Membrane With and Without Primary Closure

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
University of Louisville · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study is designed to compare the clinical and histologic results of ridge augmentation with and without primary closure over the barrier membrane. The hypothesis is that there will be no difference in crestal ridge width between the two groups.

Detailed description

A maximum of 30 patients will be selected that meet the following criteria: Inclusion Criteria 1. At least a one tooth area with a ridge defect, treatment planned to receive a dental implant. The site must be bordered by at least one tooth. 2. Healthy person that is at least 18 years old. 3. Patient understands and signs an informed consent approved by the University of Louisville Human Studies Committee. Exclusion Criteria 1. Patients with debilitating systemic diseases, diseases that affect the periodontium, or psychological problems that would interfere with treatment. 2. Previous head and neck radiation or chemotherapy within the previous 12 months. 3. Patients with known allergy to any of the materials that will be used in the study. 4. Smokers. 5. Patients who need prophylactic antibiotics prior to dental procedures. 6. Patients on long-term steroid therapy or oral bisphosphonates \> 3 years or any IV biosphosphonates. 7. Patients who are pregnant.

Conditions

Interventions

TypeNameDescription
PROCEDUREWith primary closureA cancellous block allograft will be placed for ridge augmentation and covered with a barrier membrane. The soft tissue will be primarily closed over the membrane.
PROCEDUREWithout primary closureA cancellous block allograft will be placed for ridge augmentation and covered with a barrier membrane. The soft tissue will not be primarily closed over the membrane.

Timeline

Start date
2013-09-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2013-07-17
Last updated
2016-12-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01901783. Inclusion in this directory is not an endorsement.