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Recruiting NCT07177521

Primary Stability and Peri-implant Outcomes of Short Implants in Post-extraction Single-tooth Sites

No phase Interventional Edentulous Jaw Tooth Loss Toothless Mouth

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Insertion of implants in post-extraction tooth.
Who it may be relevant to
Registry conditions: Edentulous Jaw, Tooth Loss, Toothless Mouth. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Primary Stability and Peri-implant Outcomes of Short Implants in Post-extraction Single-tooth Sites: a Randomized Controlled Trial.

Overview

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.

Interventions

  • Procedure Insertion of implants in post-extraction tooth
    Two 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 morp

Primary outcome measures

  • Primary stability [Time frame: 1 month]
Secondary outcome measures (2)
  • Clinical Indices [Time frame: 12 months]
  • Clinical Indices [Time frame: 12 month]

Eligibility criteria

Inclusion criteria

  • 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.
  • Written informed consent.

Exclusion criteria

  • Heavy smoking (>20 cigarettes/day).
  • Uncontrolled diabetes or systemic conditions affecting bone healing.
  • Current bisphosphonate/antiresorptive therapy.
  • Immunosuppression, pregnancy.
  • Poor oral hygiene or acute infection at site.
  • Severe bone dehiscence preventing primary stability.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Italy · 1 center
  • University of Bari Aldo Moro — Bari

Identifiers

NCT: NCT07177521 · Post-extraction-implants

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗