Clinical Trials Directory

Trials / Completed

CompletedNCT03205800

Temporary Anchorage Devices for Ridge Preservation

The Use of Temporary Anchorage Devices for Ridge Preservation After Tooth Extraction

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

Summary

Alveolar bone is a bony portion surrounding the root of a tooth. The alveolar bone disappears gradually when the tooth is extracted. This bone loss often becomes a problem if a patient wants to close the missing tooth space with orthodontic treatments (braces), or to get a dental implant (a metal post replacing a tooth). Therefore, we would like to place small screws at the extraction sites to preserve the alveolar bone when the teeth need to be extracted and a patient cannot start treatments some time. Mini-screws (small metal screws) are routinely used for regular orthodontic treatment. We will recruit patients who require extractions of two upper small molars (maxillary premolars) on both right and left sides. We will place one mini-screw on one side while the other side will be untouched after teeth extractions. Both sides will be followed at 8 months for examinations.

Detailed description

The purpose of this study is to investigate the effects of transcortical mini-screws on ridge preservation following tooth extraction with a split mouth design. The study will evaluate clinical and radiographic outcomes following transcortical screw placements at extraction sites compared to non-treated extraction sites. Specific Aim 1: To evaluate the clinical outcomes between the treated sites with a transcortical screw (the experimental group) and the non-treated sites (the control group) Null Hypothesis: There will be no differences in clinical parameters between the two groups. Approach: The investigators will conduct a prospective split-mouth design clinical study. The investigators will compare the clinical changes in vertical bone height and horizontal bone width at 8 months from baseline (tooth extraction). Specific Aim 2: To evaluate the radiographic outcome between the experimental group and the control group Null Hypothesis: There will be no difference in alveolar ridge height and width between the two groups. Approach: The study will measure ridge height and width using cone beam computed tomography (CBCT) at baseline and 8 months.

Conditions

Interventions

TypeNameDescription
DEVICEMini-screwPlacement of a mini-screw

Timeline

Start date
2018-01-12
Primary completion
2020-11-09
Completion
2020-11-09
First posted
2017-07-02
Last updated
2025-02-19
Results posted
2025-02-19

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03205800. Inclusion in this directory is not an endorsement.