An accuracy of computer guided surgery for one-piece ceramic implant in the anterior region single tooth replacement

Not Applicable

Completed

• Conditions: accuracyone- piece ceramic dental implantaestheticcomputer- guided software; accuracy; one- piece ceramic dental implant; aesthetic; computer&#45

• Registration Number: TCTR20170322002
• Lead Sponsor: Faculty of Dentistry Mahidol university

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2017-02-28
• Study Start: 2017-03-22
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Inclusion criteria
•The participant should be in the age of 20-85 years old.
•The participant should be healthy or well-controlled systemic disease.
•The participant should be in need of an implant-supported single tooth prosthesis in the incisor area
•The participant should have adequate bone for placing an implant of 3.3 mm in diameter and at least 8 mm in length to obtain primary stability. However, the contour bone augmentation with synthetic bone materials simultaneously with implant placement is allowed.
•The participant should have a stable occlusal relationship.
•The implant site should be healthy without sign of residual infection.
•The one-piece ceramic implant can be placed in the ideal position according to the prosthesis and available bone without abutment preparation.

Exclusion Criteria

•Smoking of more than 10 cigarettes per day.
•Pregnancy.
•The participant with psychiatric disorder or unable to give his/her informed consent to participate.
•The participant with a history of radiation therapy at head and neck area.
•The participants with untreated chronic periodontitis or un-controlled chronic periodontitis.
•The participant who has an inadequate inter-occlusal space for cement-retained restoration.
•The participant who has anterior deep bite occlusion.
•The participant who has history and sign of parafunctional habits including clenching, bruxism.
•The participant who has inadequate bony architecture to obtain primary stability and required major bone augmentation.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Deviation of dental implant position N/A Using coDiagnostic Software

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A