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Clinical Trials/NCT03205800
NCT03205800CompletedNot Applicable

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

University of Maryland, Baltimore1 site in 1 country6 target enrollmentStarted: January 12, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
6
Locations
1
Primary Endpoint
Changes in Width of Extraction Site (Ridge)

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •age ≥ 18 years
  • •two maxillary premolars (left and right) required to be extracted based on recommended dental treatment plans

Exclusion Criteria

  • •uncontrolled hypertension
  • •diabetes mellitus
  • •subjects with a history of a long-term use of corticosteroid (> 6 months)
  • •subjects with a history of taking oral/IV bisphosphonates within the past 2 years

Arms & Interventions

Mini-screw placement

Experimental

One mini-screw (8 mm length) will be placed at the buccal plate of the extraction socket one week after the atraumatic extraction of maxillary first or second premolars in one side.

Intervention: Mini-screw (Device)

No treatment

No Intervention

No treatment will be conducted on the contralateral side.

Outcomes

Primary Outcomes

Changes in Width of Extraction Site (Ridge)

Time Frame: 8 months

the distance from the buccal plate to the palatal plate

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Se-Lim Oh

Assistant Professor

University of Maryland, Baltimore

Study Sites (1)

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