K08.1
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Signed informed consent form - Good general health - Need of one implant in healed posterior sites (premolar or molar) - Need of a single implant-supported crown in the non-aesthetic area - Presence of antagonists
Exclusion criteria
Exclusion criteria: - Women who are pregnant at time of implant placement - Heavy smokers - Poor oral hygiene (plaque index > 30 %) - Active periodontal disease - Secondary exclusion criteria (to be applied at Visit 2): The presence of a buccal dehiscence defect height exceeding 5 mm
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiographic bone level after 5 years | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints will be assessed after 0.5, 1, 3 and 5 years: - Biological: Implant survival rate, marginal bone level, bleeding on probing, mucosal recession - Technical: Crown survival, wear of the crown and the antagonist - Patient related: Pain evaluation form | — |
Countries
Switzerland
Contacts
Universität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin