Lithium Disilicate (CAD/CAM) Fixed Partial Dentures (FPD) Clinical Study

Missing Tooth Clinical Trial

Official title:

Clinical Evaluation of Chairside Computer Assisted Design/Computer Assisted Machining (CAD/CAM) Lithium Disilicate Fixed Partial Dentures (FPD)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03036566
• Other study ID #: HUM00081086
• Status: Terminated
• Phase: N/A
• Start date: March 2014
• Est. completion date: March 5, 2020

Study information

• Verified date: March 2023
• Source: University of Michigan
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This investigation will be a clinical trial to study the performance of a high strength ceramic material for bridges to replace missing teeth. The ceramic material has been approved by the FDA for patient treatment. A computer technique will be used to make the bridges. The bridges will be cemented using an adhesive resin cement (MultiLink Automix/Ivoclar). The bridges are planned be evaluated for clinical performance at 6 months, 1 year, 2 years, 3 years, and if funding permits, 4 years, and 5 years. The purpose of the study is to measure how well the high strength bridges function over an extended period of time.

Description:

The study will be composed of 30 bridges placed in adult patients that have been identified as requiring replacement of a single tooth. All the bridges will be made from the same high strength ceramic material (emaxCAD/Ivoclar) using a computer to make the entire bridge. All the crowns will be cemented using the most current marketed version of the manufacturer's adhesive resin cement (MultiLink Automix/Ivoclar). At each recall appointment an evaluation of the bridge will be completed as well as clinical photographs, an intraoral digital scan, and impression of the bridge. The purpose of the study is to measure how well the high strength bridges function over an extended period of time.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 30
• Est. completion date: March 5, 2020
• Est. primary completion date: March 5, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• missing one anterior or premolar tooth that is appropriate for replacement with a bridge. The second premolar tooth will be the most distal tooth acceptable as a pontic for inclusion in the study.

• healthy periodontal status for the adjacent abutment teeth with 1:1 crown:root ratio

• abutment teeth must be asymptomatic prior to treatment

• Endodontically treated teeth will be acceptable for abutments as long as nonmetallic cores can be placed to retain the FPD since the lithium disilicate will be bonded to the abutments.

• no more than one bridge will be placed per patient. If a patient presents with more than one missing teeth acceptable for the study, premolar teeth will be included prior to anterior teeth. Each bridge will be three units and include only one missing tooth.

Exclusion Criteria:

• sensitive abutment teeth

• teeth with a history of direct or indirect pulp capping procedures

• patients with significant untreated dental disease to include periodontitis and caries

• pregnant or lactating women

• patients with allergies to any material in the study

• patients unable to return for recall appointments

Related Conditions & MeSH terms

• Anodontia
• Missing Tooth
• Tooth Loss

Intervention

Device:
• Lithium disilicate ceramic (Ivoclar)
Three unit high strength ceramic bridges replacing a single tooth.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
University of Michigan	Ivoclar Vivadent AG

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bridge Failure	Bridge failure includes fracture of the bridge or loss of the bridge requiring placement of a new bridge at any time between delivery and five years.	from delivery of the bridge up to 5 years
Secondary	Bridge Loss of Retention	Loss of retention is measured as detachment of the bridge from the teeth without fracture of the bridge requiring recementation of the bridge.	from delivery of the bridge up to 5 years
Secondary	Tooth Sensitivity	Tooth Sensitivity is evaluated as either "0" if the subject reports that there is NO sensitivity for either tooth with the study bridge, or "1" if the subject reports that there IS tooth sensitivity to hot/cold or biting pressure for either tooth supporting the bridge. The better outcome is to have NO tooth sensitivity.	from delivery of the bridge up to 5 years
Secondary	Margin Staining	Margin Staining is evaluated as either "0" if there is NO staining at the crown margin where it meets the tooth for either tooth supporting the bridge, or "1" if there IS staining at the crown margin where it meets the tooth for either tooth supporting the bridge. The better outcome is to have NO margin staining.	from delivery of the bridge up to 5 years