Immediate Implant Placement in the Posterior Region Combining Sealing Socket Abutment and Peri-implant Socket Filling.
Recruiting
N/A
Interventional Study
Dental Implantation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 99
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 30 (estimated)
- Sponsor
- University of Liege · Other
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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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Good general health (ASA I/II),
* More than 18 years old,
* Smoker \< 10c/day, one hopeless tooth,
* Healthy periodontal condition,
* Presence of at least 2 mm of keratinized gingiva
* Intact buccal bone wall
* Adequate plaque control (FMPS ≤ 25%)
* Adequate bone quantity allo…
Contacts