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NCT06077513

Ti-Mesh Frame Comparison for Alveolar Bone Augmentation

Enrolling by Invitation
NAAges 18–80InterventionalTreatment
Boston University
~30 participants
Updated 2026-02-12 on ClinicalTrials.gov
What's tested:CAD-CAM designed and preprinted Ti-Mesh frameConventional chairside fabrication of Ti-Mesh frame

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Bone contour accuracy
Measured over 5 months post op
+2 more outcomes measured

Conditions

Tooth Loss

Explore related trials

Alveolar bone lossTooth Loss

Where it's being run

1 sites across 1 states
Massachusetts1

Study leadership

  • Serge Dibart, DMD · PRINCIPAL_INVESTIGATOR · BU Goldman School of Dental Medicine, Oral Biology/Periodontics
  • Albert M Price, DMD · STUDY_DIRECTOR · BU Goldman School of Dental Medicine, Oral Biology/Periodontics

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Partially edentulous
Adult dental patients that require moderate 3-D bone augmentation for dental implant site improvement

Exclusion

Poor oral hygiene indices for microbial plaque (PI) and gingival inflammation (GI)
Patients who have been on Chemotherapy or Radiation therapy within last 5 years.
Patients under active treatment with following medications: Bisphosphonates, Gabapentin, Glucocorticoids, Methotrexate, or Estrogen supplements.
Subjects under the direct supervision of the PI
Smoking more than 10 cigarettes per day
Uncontrolled diabetes or other metabolic disorders

What this trial measures

  • Bone contour accuracy5 months post op

    Bone contour accuracy will be derived by merger of the post op Cone beam computed tomography (CBCT) DICOM file with the CBCT-1/CEREC-1/Virtual Implant file produced at the planning stage. Accuracy of fit will be calculated for volume and linear measures (4 sides of each implant-MDBL) horizontal and vertical from the implant restorative platform.

  • Total surgical time2 hours

    Total surgical time is defined as from incision time to completion of sutures and will be measured in minutes.

  • Surgical exposure time for recipient site5 minutes

    Surgical exposure time will be measured for recipient site in minutes