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Implant Primary Stability and Ridge Dimensional Changes Utilizing the Osseodensification Protocol

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Dental Implants

Treatments

Device: OsseoDensification (OD) protocol
Device: standard drilling (SD) protocol (NobelReplace® Conical)

Study type

Interventional

Funder types

Other

Identifiers

NCT05283928
HSC-DB-21-0597

Details and patient eligibility

About

The purpose of this study is to compare ridge dimensional changes between densification and standard drilling protocols and to compare primary and secondary stability of implants placed by bone densification and standard drilling protocols

Enrollment

15 patients

Sex

All

Ages

22+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who understand and agree to this study.
  • Adequate Oral hygiene
  • One or more edentulous spaces, which are 10 weeks or longer after extractions

Exclusion criteria

  • Pregnancy.
  • Smoking of more than 5 cigarettes/day.
  • History of alcoholism or drug abuse during the last 5 years.
  • Uncontrolled Hypertension or diabetes.
  • Patient with malignant tumor.
  • Patients on daily dose of steroids.
  • Patients with history of chemotherapy or radiation for the last 12 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

15 participants in 2 patient groups

OsseoDensification (OD) protocol
Experimental group
Treatment:
Device: OsseoDensification (OD) protocol
standard drilling (SD) protocol
Active Comparator group
Treatment:
Device: standard drilling (SD) protocol (NobelReplace® Conical)

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Popi Stylianou, DDS,MS; Nikola Angelov

Data sourced from clinicaltrials.gov

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