N/A N=68 Randomized Single-blind Treatment

Performance of MicroTextured Dental Implants

Partially Edentulous Jaw

Bottom Line

View on ClinicalTrials.gov: NCT01821417 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Mar 2017

Primary outcome: Primary: Change in Millimeters of Bone Loss Surrounding the Implant Device — -0.35; -0.82 millimeters

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Microtextured dental implant treatment (Device); Dental implant treatment (Device)
Age: Adult, Older Adult · 19+ yrs
Sex: All
Sponsor: University of Alabama at Birmingham
Primary completion: Jun 2014

Outcome Measures

Outcome	Result	p-value
PRIMARY Change in Millimeters of Bone Loss Surrounding the Implant Device	-0.35; -0.82	—
SECONDARY Changes in Peri-implant Gingivitis Score	—	—
SECONDARY Millimeters of Periodontal Pocket Depth Surrounding the Dental Implant Device	—	—

Summary

The study will compare initial peri-implant bone healing and longitudinal osseointegration between a fully microtextured dental implant and an analogous implant with a smooth machined collar. The investigators hypothesize the fully textured implant will result in less peri-implant crestal bone resorption than the implant with a machined collar.

Eligibility Criteria

Inclusion Criteria

Be a current registered University of Alabama at Birmingham (UAB)dental school patient
Existence of one or more missing teeth scheduled to be replaced with dental implants
Healthy enough to undergo proposed therapy without compromising existing health
Able to consent for their own inclusion
Able to read and understand the informed consent form
Demonstrated willingness to comply with protocol requirements and timeline

Exclusion Criteria

Any health condition that in the opinion of the investigators may adversely affect bone healing
Any medication that in the opinion of the investigators may adversely affect bone healing
Any indication of an inability to make autonomous decisions
Reported pregnancy at the time of enrollment -

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01821417). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.