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The purpose of the study is to test whether a two-piece zirconia implant is as reliable in the indication of immediate implant placement as a standard titanium implant.
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Inclusion criteria
Patients giving informed consent to participate in the clinical trial and fulfil the following criteria will be included in the investigation:
Exclusion criteria
Primary exclusion criteria are as follows:
parafunctional habits;
active periodontitis;
smoking;
pregnancy;
acute or chronic medical conditions for which implant therapy has always been considered a contraindication: uncontrolled diabetes (HbA1c >8.0%), mucosal disease, untreated periodontitis, immunological disorders, active malignancy, alcoholism, condition after radiation therapy to the head and neck area and antiresorptive therapy.
Secondary exclusion criteria will be applied at surgical procedure:
loss of facial bone wall due to extraction procedure;
insufficient primary stability (less than 32Ncm insertion torque).
Primary purpose
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Interventional model
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33 participants in 2 patient groups
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Central trial contact
Michael Payer, DDS; Marlene Lindner, DMD
Data sourced from clinicaltrials.gov
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