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

An Accuracy Study of one-piece ceramic dental implantation in anterior teeth replacement using a computer guided surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170322002
Enrollment
Unknown
Registered
2017-03-22
Start date
2016-03-21
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

accuracy one&#45

Interventions

One&#45
piece ceramic dental implant placed by using computer guided software.
Experimental Device

Sponsors

Faculty of Dentistry Mahidol university
Lead Sponsor
Institute Straumann AG
Collaborator

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
Deviation of dental implant position N/A Using coDiagnostic Software—

Secondary

MeasureTime frame
N/A N/A N/A—

Countries

Thailand

Contacts

Public ContactNopparat Suksod

Faculty of dentistry Mahidol University

w.suksod@gmail.com0835435669

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026