Five Year Survival Study Evaluating the Genesis Dental Implant System

Dental Implants Clinical Trial

— Genesis Dental  

Official title:

Clinical Analysis of a Biomimetic Implant System: Five Year Survival Rates, Marginal Bone-level Changes, and Soft Tissue Aesthetics.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01573026
• Other study ID #: KD-CR 02
• Status: Active, not recruiting
• Phase: N/A
• First received: April 4, 2012
• Last updated: April 5, 2012
• Start date: August 2011
• Est. completion date: July 2017

Study information

• Verified date: April 2012
• Source: Keystone Dental, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The purpose of this research study is to document the use if the Keystone Dental Genesis Dental Implant System in standard clinical use and to provide 5 year survival data.

Description:

The technology behind dental implants is well established and the Genesis Dental Implant System has been cleared for marketing by the FDA. It is Keystone Dental's choice to collect post-market data within the framework of a clinical trial in order to assess the clinical performance of this device.

The risks of the Genesis Dental Implant System are no different than other comparable dental implant systems currently in use. Keystone Dental expects the clinical performance of this device to be equal to that of comparable implant systems.

The purpose of this research study is to assess the 5 year survival rate of the Genesis Dental Implant System, as well as assess the safety and effectiveness endpoints, which include incidence of adverse effects, change in bone height and soft tissue aesthetic outcomes.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 120
• Est. completion date: July 2017
• Est. primary completion date: March 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• Subject must be between 18 and 85 years old, inclusive, and have passed growth maximum at the time of implant placement

• Subject must be willing to sign the informed consent document and adhere to study procedures.

• Subject must have one or more natural teeth missing or about to be extracted.

• Subject must fulfill all the accepted medical and dental requirements for treatment with dental implants.

• Subject must desire treatment with dental implants.

Exclusion Criteria:

• Subject refuses to sign the informed consent document.

• Subject's treatment success by both clinical and esthetic measures may be compromised by the restricted range of product available for the study.

• The treatment plan to use the range of products available is not in the best interests of the subject. Please see Section 1.2.1 for restrictions on product availability.

• The implant site(s) had a previously failed implant.

• Subject cannot be treated within the restrictions of the treatment plan laid out in Section 5. In addition, please see Section 1.2.1 for restrictions on product availability.

• Subject with alveolar ridge dimensions that are not sufficient to accommodate and sustain proper implant placement.

• Subject is not communicable in an understandable language.

• Current Alcohol or Drug Abuse (within previous 12 months) as noted in the subject's chart.

• Women who are pregnant at time of enrollment in to the study.

• Subject with out of control metabolic disease.

• Subject who have been on chemotherapy or long term cortisone use (at any time).

• Subject with known allergy to titanium.

• Subject with diabetes.

• Subject with a history of autoimmune disease (e.g. documented multiple allergies, systemic lupus erythematosus, dermatomyositis, etc.) or immunosuppressive disease (e.g. human immunodeficiency virus or acquired immunodeficiency syndrome).

• Subject with epilepsy.

• Subjects with uncontrolled or severe cases of hyperthyroidism, malignancies, renal disease, liver problems, hypertension, leukemia, severe vascular heart disease, hepatitis, collagen and bone diseases, or other serious illnesses.

• Subject currently taking bisphosphonate or calcium channel blockers.

• There is reasonable doubt that the subject will comply with the recall schedule.

• There is reasonable doubt that the subject will comply with the clinicians' instructions.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Dental Implants

Locations

Country	Name	City	State
United States	Kevin G. Murphy & Associates, PA	Baltimore	Maryland
United States	Dental Design	Gainesville	Virginia
United States	PerioHealth Professionals, PLLC	Houston	Texas
United States	Specialized Dentistry of New York	New York	New York
United States	Newport Coast Oral Facial Institute	Newport Beach	California
United States	Periodontal Medicine & Surgical Specialists, LTD	Oakbrook Terrace	Illinois
United States	Edwin Rosenberg, DMD, HDD, BDS	Philadelphia	Pennsylvania
United States	Brighton Periodontal & Implant Dental Group	Woodland Hills	California

Sponsors (4)

Lead Sponsor	Collaborator
Keystone Dental, Inc.	Aptiv Solutions, CadBlu North (Hastings, MN), Pirkka Nummikoski, DDS, MS

Country where clinical trial is conducted

United States,