Primary Stability and Peri-implant Outcomes of Short Implants in Post-extraction Single-tooth Sites
NCT ID: NCT07177521
Last Updated: 2026-01-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
10 participants
INTERVENTIONAL
2025-01-10
2026-08-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Immediate Implants Inserted Through Open Flap, Open Flap and Bone Grafting and Flapless Techniques
NCT03001752
X-space Implants in Post-extraction Sites.
NCT04492111
Short Implants in Atrophic Posterior Maxilla
NCT06759246
Osteoimplant and Dental Implants Stability
NCT06657521
Comparative (Short vs. Standard) Length Implants in Early Stability Patterns.
NCT07162389
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group 1
Socket grafting with a fully resorbable synthetic biomaterial (β-tricalcium phosphate + calcium sulfate).
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 morphometric analysis.
Group 2
Socket grafting with a xenograft and a custom Sealing Socket Abutment with a concave emergence profile.
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 morphometric analysis.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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 morphometric analysis.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
18 Years
75 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Bari Aldo Moro
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Giuseppe D'Albis
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Giuseppe D'Albis, Dr
Role: PRINCIPAL_INVESTIGATOR
University of Bari Aldo Moro
Saverio Capodiferro, Prof
Role: STUDY_CHAIR
University of Bari Aldo Moro
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Bari Aldo Moro
Bari, , Italy
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Post-extraction-implants
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.