Commercially pure (CP) titanium is the gold standard to produce dental implants because it has a huge volume of scientific publications over a period of more than 50 years, it is cheap and simple to produce (i.e., making dental implants economically "affordable") and comes in numerous specific designs of screws for various indications. That is why more than 95% of the implant market is dominated by titanium. However, there is an innovation trend to manufacture implants from more inert and biocompatible materials. Ceramic implants represent a valuable alternative for expanding the patient base of clinicians, especially in cases with challenging aesthetic demand. Furthermore, there has been a significant increase in the number of patients requesting metal-free dentistry or bio-holistic implant treatments. In the past, ceramics were often branded as "inferior" quality due to its reputation as being brittle but the growing volume of scientific publications specifically on zirconia are demonstrating that it is comparable in fracture-strength with titanium implants. There is a clear market niche for zirconia implants, especially in cases of: * Aesthetic reconstructions in the anterior region, especially in patients with a thin gingival biotype * Gingival recessions where a white colored implant is a great advantage * For patients with a titanium intolerance/sensitivity * For patients who prefer a bio-holistic/metal-free dental approach. Today, clinicians are asking for long-term clinical results of zirconia as a dental implant material. Therefore, Z-Systems AG is conducting this zirconia dental implant registry. A registry design was chosen because it will capture long-term benefits/risks from clinical routine without patient selection.
Study Type
OBSERVATIONAL
Enrollment
240
This is an observational study, collecting data on the use of Z5-BL Dental Implants.
This is an observational study, collecting data on the use of Z5-BL Dental Implants.
MVZ Stiller GmbH
Berlin, Germany
RECRUITINGGemeinschaftspraxis Börner, Hagen
Köpenick, Germany
RECRUITINGPraxis dentblanche AG
Solothurn, Grenchen, Switzerland
RECRUITINGPraxis am Klosterplatz
Olten, Switzerland
RECRUITINGHeilPraxis - ZahnMedizin
Sankt Gallen, Switzerland
RECRUITINGAbsence of persistent subjective complaints
Absence of persistent subjective complaints such as pain, foreign body sensation and/or dysesthesia
Time frame: 12 months post-loading final prostheis
Absence of peri-implant infection
Absence of peri-implant infection with suppuration
Time frame: 12 months post-loading final prostheis
Absence of mobility
Absence of mobility of dental implant
Time frame: 12 months post-loading final prostheis
Frequency of occurrence of device related Adverse Device Events (ADEs) and Serious Adverse Device Events (SADEs).
Secondary Safety Outcome is frequency of occurrence of device related Adverse Device Events (ADEs), Serious Device Events (SADEs). Measured by asking patient if any adverse events occured since last follow-up.
Time frame: At implant surgery, 3 months, 6 months, 1-5 years post-loading with the final prosthesis (i.e., at every follow-up visit after implant surgery)
Exploratory outcomes - complaints and incidence
Rate of complaints and incidents related to the medical device during the whole registry.
Time frame: At implant surgery, 3 months, 6 months, 1-5 years post-loading with the final prosthesis (i.e., at every follow-up visit after implant surgery)
Exploratory outcomes - clinical satisfaction
Clinical satisfaction measured on a Likert scale: 1 to 6, with 1 being "not satisfied at all" to 6 being "highly satisfied.
Time frame: At implant surgery, 3 months, 6 months, 1-5 years post-loading with the final prosthesis (i.e., at every follow-up visit after implant surgery)
Exploratory outcomes - patient satisfaction
The patient's assessment of function and aesthetics is recorded by his/her assessment of function, aesthetic appearance, implants, speech and self-confidence. The parameters are assessed by rating the degree of satisfaction on a 100 mm Visual Analogue Scale (VAS).
Time frame: At implant surgery, 3 months, 6 months, 1-5 years post-loading with the final prosthesis (i.e., at every follow-up visit after implant surgery)
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