Skip to content

Ridge Preservation Following Tooth Extraction

Use of a Titanium Bone Screw for Ridge Preservation Following Tooth Extraction

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05485194
Enrollment
0
Registered
2022-08-03
Start date
2025-12-01
Completion date
2028-03-31
Last updated
2025-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Resorption, Tooth Extraction

Brief summary

An animal study and our pilot human study demonstrated that placing a smooth-surface titanium bone screw (TBS) over the buccal plate of an extraction socket resulted in less dimensional changes of the alveolar ridge along with no adverse effects. The purpose of this randomized clinical trial is to investigate the effectiveness of TBS application for ridge preservation in comparison to (1) unassisted/non-interventional socket healing and (2) alveolar ridge preservation (ARP) approach using allografts and a membrane.

Detailed description

The participants will be randomized to one of the three groups: the non-intervention, titanium bone screw (TBS), and alveolar ridge preservation (ARP) groups. The sockets in the non-intervention group will be filled with blood clots only. One TBS will be placed over the labial/buccal plate of the extraction socket in the TBS group on the same day of the extraction. Allograft and resorbable collagen membrane will be used for the ARP group.

Interventions

OTHERReducing dimensional changes following tooth extraction

Use of a titanium bone screw for ridge preservation following tooth extraction

Sponsors

University of Maryland, Baltimore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* age ≥18 years * a tooth, which is in the area from the central incisor to the second premolar bounded by teeth (or implants) mesiodistally * a tooth requiring extraction

Exclusion criteria

* thyroid dysfunctions * diabetes mellitus * history of a chronic use of corticosteroids (\>6 months) * history of oral/intravenous bisphosphonates within the past 2 years * smoking * history of other systemic conditions that could affect bone integrity.

Design outcomes

Primary

MeasureTime frameDescription
The width of the alveolar boneup to 6 monthsDimensional changes in the width of the alveolar bone following tooth extraction

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026