Template-guided implantation of one-piece ceramic implants.A prospective clinical pilot study.

Not Applicable

• Conditions: K08.1; Loss of teeth due to accident, extraction or local periodontal disease

• Registration Number: DRKS00012927
• Lead Sponsor: niversitätsklinikum Ulm/Studienleiter: Prof. Dr. Ralph G. Luthardt, Klinik für Zahnärztliche Prothetik

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-09-07
• Study Completion: 2017-12-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

Gaps in the upper and / or lower jaw tooth area
Free-ending situations in the upper and / or lower jaw area
The extraction is at least 3 months. Only early implantations (3 - 6 months post-extraction) and late implantation (> 6 months post-extraction) are performed.
The template must be applied to the tooth. For this purpose, more than 5 residual teeth must be present in the jaw to be implanted.
The patient has good oral hygiene and compliance.
A preimplantological hygiene phase must be completed.
Patient's consent.

Exclusion Criteria

Persons under 18 or not legally competent persons
Untreated acute periodontitis with pocket depths> 4 mm.
Strong smokers (more than 10 zig / d)
Taking bisphosphonates
Pregnant
Alcohol or drug addicts
Patients with an infectious disease such as hepatitis or HIV or AIDS
Patients with severe diabetes m.
immediate implantation
Width of the gap in the mesio-distal direction with single tooth gaps> 7.1 mm.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Deviation of the planned implant position from the actual position. The deviation is described by the distance at the crestal implant penetration point, at the apical end of the implant, at the height of the implant and in the axis deviation. The measurement will be performed immediately after insertion of the implant.

Secondary Outcome Measures

Name	Time	Method
Indication limitations for the stencil design of 2ingis.<br>Clinical complications: Insufficient template content, eg.<br>Technical complication: stencil fracture or the like.<br><br>Feasibility study for a subsequent multicentric field study.<br>The feasibility study should give evidence of a sufficient clinical accuracy of the used templates and work out possible indication restrictions.<br><br>All recordings are made on the day of Implantation. No further follow-up is performed.<br>