Immediate Implant Placement in the Posterior Region Combining Sealing Socket Abutment and Peri-implant Socket Filling.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUniversity of Liege

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

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators