About this trial
The placement of short implants in post-extraction sockets is a valuable option when residual bone height is limited, minimizing morbidity and treatment time. The management of the peri-implant gap and soft tissues may influence primary stability, hard/soft tissue remodeling, and implant success.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age ≥18 years.
Single-tooth post-extraction sites requiring immediate implant placement in posterior regions (premolars/molars) or selected anterior sites.
Planned short implant (≤7-8 mm length, 3.5-5.0 mm diameter).
Adequate oral hygiene, no active periodontal disease.
Disqualifiers
Heavy smoking (>20 cigarettes/day).
Uncontrolled diabetes or systemic conditions affecting bone healing.
Current bisphosphonate/antiresorptive therapy.
Immunosuppression, pregnancy.
Trial design
Parallel
Treatments tested in this trial
Insertion of implants in post-extraction tooth
Procedure/SurgeryTwo widely used approaches include: 1. Socket grafting with a fully resorbable synthetic biomaterial (β-tricalcium phosphate + calcium sulfate). 2. Socket grafting with a xenograft and a custom Sealing Socket Abutment (SSA) with a concave emergence profile. No randomized controlled trials have yet compared these protocols with integrated outcomes including resonance frequency analysis, peri-implant health indices, radiographic bone level changes, and digital intraoral scanning (IOS)-based morphometric analysis.
Treatment groups
Trial outcomes
Primary outcomes
Primary stability
To compare the primary stability (ISQ values at implant insertion) of short implants placed in post-extraction sockets using the two grafting protocols.
Secondary outcomes
Clinical Indices
To assess peri-implant health indices (PD)
Clinical Indices
To assess peri-implant health indices (BoP)
Sponsors and contacts
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