Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
Healthy Volunteers
NCT07177521

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

Led by University of Bari Aldo Moro · Updated on 2026-01-27

10

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Single-tooth post-extraction sites needing immediate implant placement in posterior regions (premolars/molars) or selected anterior sites
  • Planned use of a short implant (7-8 mm length, 3.5-5.0 mm diameter)
  • Adequate oral hygiene with no active periodontal disease
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Heavy smoking (more than 20 cigarettes per day)
  • Uncontrolled diabetes or systemic conditions affecting bone healing
  • Current bisphosphonate or antiresorptive therapy
  • Immunosuppression or pregnancy
  • Poor oral hygiene or acute infection at the implant site
  • Severe bone loss preventing primary implant stability

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Bari Aldo Moro

Bari, Italy, 70021

Actively Recruiting

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Research Team

G

Giuseppe D'Albis, Dr

CONTACT

S

Saverio Capodiferro

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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