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Study identifier: NCT05741749 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Dental Implantation  ·  Sponsor: University of Liege

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Bruno De Carvalho, DDS, Ms, PhD Fellow  ·  +32479510961  ·  bruno.decarvalho@chuliege.be

Always discuss trial participation with your own doctor first.

Locations (1)

CHU de LiègeLiège, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT05741749