Comparing Conventional Dental Implants and Trabecular Metal™ Dental Implants After Sinus Floor Elevation

Harvard Medical School (HMS and HSDM)

Status: Completed

Conditions: Atrophy of Edentulous Alveolar Ridge; Partial Edentulism

Treatments: Device: Two implant designs in a Sinus Bone Augmentation Procedure; Device: Two implant designs in a Sinus Floor Elevation Procedure

Study type: Interventional

Funder types: Other

Identifiers

NCT02404649

HarvardMS

Details and patient eligibility

About

This is a research study to test the clinical outcome of Trabecular Metal™ Dental Implants (TMDI) (Zimmer Dental Inc Carlsbad, CA, US) in the Maxillary Sinus region. This project will enroll 30 active subjects who will receive two dental implants in the edentulous maxillary molar region. This 24-month research study will examine the clinical stability of TMDI in both sinus elevation and sinus augmentation environments. The proposed research lays the foundation for improved health care by providing surgeons and restorative dentists with data for determining the effects TMDI have on clinical success in less than optimal osseous environments. The rationale that underlies the investigation is that identification of the influences of trabecular surface design on implant stability in varying bone types will allow routine, predictable use of early loading, which, in turn, will translate into more rapid, economical health care, and improved psychosocial well-being of the patient. If these hypotheses are correct, the results are expected to provide evidence based research data to support early loading and immediate loading of single implants in sites of adequate bone volume, and density with or without the use of graft materials in sinus lift procedures. In addition, it is expected that these results will fundamentally advance the field of implant dentistry and bioengineering by providing information on the principles of the bone density-mechanical environment-implant stability interaction.

Full description

Specific Aims

Primary Outcome Measures:

• The objective of this study is to allow a preliminary analysis of the resonance frequency values over the 12 month period, which will be the primary outcome

Secondary Outcome Measures:

• To assess Crestal bone level maintenance

Study Arms Bone Augmentation: Placement of two dental implants in Sinus augmented with Puros Cortico-Cancellous Particulate Allograft (70% Cortico and 30% Cancelleous) (Zimmer Dental- Carlsbad, CA, USA)- one implant will be TMDI (Zimmer Dental- Carlsbad, CA, USA) and the second will be Tapered Screw-Vent TSV-MTX (Zimmer Dental- Carlsbad, CA,USA). Implant stability will be determined by the initial insertion torque and RFV values at time of implant placement and after 1 month of healing on a monthly basis up until 12 months post implant placement.

Sinus Elevation only: Placement of two dental implants as mentioned above in sinus augmented by sinus elevation procedure, blood clot and CopiOs Pericardium Membrane (Zimmer Dental- Carlsbad, CA, USA) only. One implant will be TMDI (Zimmer Dental- Carlsbad, CA, USA) and the second will be Tapered Screw-Vent TSV-MTX (Zimmer Dental- Carlsbad, CA,USA). Implant stability will be determined by the insertion torque and RFV values at time of implant placement and after 1 month of healing on a monthly basis up until 12 months post implant placement.

Enrollment: 33 patients

Sex: All

Ages: 21 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• • The subject male or female between 21-75 years of age and has:

  • The ability to understand and sign the informed consent prior to starting the study
  • The ability and willingness to comply with all study requirements
  • Adequate oral hygiene
  • The presence of a atrophic, pneumatized, partially edentulous maxilla requiring a lateral approach technique
  • Adequate bone volume to accommodate the planned endosseous dental implant (e.g. sufficient height of bone (5 mm or greater) such that the implant would achieve primary stability, and sufficient width that the implant could be placed within the confines of the existing bone without dehiscence or fenestration. The only implant length utilized in this protocol will be a 10 mm long TMDI (Zimmer)
  • Existing teeth that are healthy and adequately restored, and desired a fixed restoration on implants
  • had a negative pregnancy test within one week prior to surgery, if of childbearing potential.

Exclusion criteria

• Subjects who have smoked cigarettes or chewed tobacco within the past year
• History of alcoholism or drug abuse within the past 5 years
• Subjects with Severe bruxing or clenching habits
• Untreated periodontitis
• Subjects at undue risk for an outpatient surgical procedure
• Subjects with the presence of residual roots at the implant site
• Subjects with history of site development (extensive bone augmentation) at the implant site in the past 4 months
• Placement of implant in an extraction site that had been healing for less than 2 month
• Presence of local inflammation or mucosal diseases such as lichen planus
• Subjects with uncontrolled diabetes (defined as HA1c > 7.0 percent)
• Subjects with current hematologic disorder or chronic use of Coumadin (or similar) anti-coagulant therapies
• Subjects with history of leukocyte dysfunction and deficiencies
• Subjects with Metabolic bone disorders
• Subjects with history of renal failure
• Subjects with history of liver disease
• Immunocompromised Subjects having HIV, RA, SLE or other collagen vascular disorders
• Subjects with chronic corticosteroid use
• Subjects undergoing chemotherapy
• Subjects with a history of use of IV-based bisphosphonates
• Subjects with history of radiation treatment to the head or neck
• Subjects requiring grafting of bone or mucosal tissue at the time of implant placement, which would require submersion of the implant during the healing period
• Subjects using of any investigational drug or device within the 30 day period immediately prior to implant surgery
• Pregnant women or women intending to become pregnant during this study period.
• Subjects requiring submersion of implants for esthetic reasons

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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33 participants in 2 patient groups

Bone Augmention

Active Comparator group

Description:

Two implant designs in a Sinus Bone Augmentation Procedure. Sinus bone augmentation with Puros Cortico-Cancellous Particulate Allograft (70% Cortico and 30% Cancelleous) (Zimmer Dental- Carlsbad, CA, USA)- one implant will be TMDI (Zimmer Dental- Carlsbad, CA, USA) and the second will be Tapered Screw-Vent TSV-MTX (Zimmer Dental- Carlsbad, CA,USA). Implant stability will be determined by the initial insertion torque and RFV values at time of implant placement and after 1 month of healing on a monthly basis up until 12 months post implant placement.

Treatment:

Device: Two implant designs in a Sinus Bone Augmentation Procedure

Sinus elevation only

Active Comparator group

Description:

Two implant designs in a Sinus Floor Elevation Procedure. Placement of two dental implants as mentioned above in sinus bone augmentation by sinus elevation procedure, blood clot and CopiOs Pericardium Membrane (Zimmer Dental- Carlsbad, CA, USA) only. One implant will be TMDI (Zimmer Dental- Carlsbad, CA, USA) and the second will be Tapered Screw-Vent TSV-MTX (Zimmer Dental- Carlsbad, CA,USA). Implant stability will be determined by the insertion torque and RFV values at time of implant placement and after 1 month of healing on a monthly basis up until 12 months post implant placement.

Treatment:

Device: Two implant designs in a Sinus Floor Elevation Procedure