About this trial
The primary endpoint of this study is to compare the soft tissue contour changes after immediate implant placement combined to peri-implant socket filling with a sealing socket abutment (SSA) versus a standard healing abutment. The hypothesis is that the SSA better preserves the alveolar ridge profile in the cervical region compared to a conventional healing abutment. The secondary objectives aim to evaluate 3D hard tissue changes, peri-implant bone remodeling, soft tissue health, esthetic outcomes and the patients related outcome measures.
Eligibility criteria
Qualifiers
Good general health (ASA I/II),
More than 18 years old,
Smoker < 10c/day, one hopeless tooth,
Healthy periodontal condition,
Disqualifiers
Auto-immune disease or immunocompromised patients
Uncontrolled diabetes
Use of steroids or biphosphonates
Local or systemic infection (medical treatment needed prior to entrance to the study)
Trial design
Treatments tested in this trial
- Socket Seal Abutment