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Short Implants in Atrophic Posterior Maxilla

U

University of Bari Aldo Moro

Status

Completed

Conditions

Bone Atrophy, Alveolar
Edentulism
Sinus Pneumatization

Treatments

Procedure: implant placement

Study type

Interventional

Funder types

Other

Identifiers

NCT06759246
Implants01

Details and patient eligibility

About

This study aims to evaluate the clinical and radiological outcomes of short implants in the rehabilitation of single-tooth edentulism in the posterior maxilla. By assessing these outcomes, the research seeks to determine the effectiveness and long-term viability of short implants as a minimally invasive solution, particularly in cases where bone height is limited.

Full description

The present municentric retrospective study was conducted following the STROBE statement recommendations for observational studies and in compliance to the principles of the Declaration of Helsinki on clinical research involving human subjects.The study aims to evaluate short implants placed over the past 15 years by three experienced clinicians, assessing their survival and clinical success. Specifically, the study collects clinical data such as probing depth, the presence or absence of peri-implantitis, and radiological findings.

Enrollment

150 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Good health status according to the classification system of the American Society of Anesthesiology (ASA), and patients were required to be 18 years of age or older.
  • No general medical condition that would contraindicate implant therapy.
  • No active periodontal disease, defined as a periodontal probing depth of less than 4 mm, or previously treated periodontitis.
  • Good oral hygiene, with a full-mouth plaque index of less than 25%.
  • Adequate control of inflammation, with a full-mouth bleeding on probing (BOP) of less than 25%.

Exclusion criteria

  • Smoking more than 15 cigarettes per day
  • Presence of untreated periodontal disease
  • Pregnancy or breastfeeding at the time of enrollment
  • Active infections
  • Less than 2 mm of keratinized mucosal tissue.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

150 participants in 1 patient group

Atrophic maxillae
Other group
Description:
A group of patients with atrophic maxillae requiring rehabilitation for single-tooth edentulism.
Treatment:
Procedure: implant placement

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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