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OpenTrials
Completed

NCT Number: NCT06759246

Short Implants in Atrophic Posterior Maxilla

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Bari Aldo Moro

Bari, 70021, Italy

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

implant placement

Procedure

Placement of short implants for the rehabilitation of single-tooth edentulism in atrophic maxillae near the maxillary sinus.

Primary outcomes

  1. Clinical outcome

    Time frame: 2 years

    Survival rate: A statistical analysis will be conducted to evaluate the implant survival rate at three specific time points: T1 (3 months), T2 (6 months), and T3 (2 years).

Secondary outcomes

  1. Rx outcome

    Time frame: 2 years

    Radiographic measurements will be obtained using standardized imaging techniques. The measurements will be performed digitally using dedicated three-dimensional radiological imaging software, ensuring high precision. Distances will be measured in millimeters to evaluate implant positioning, bone levels, and defect morphology with accuracy.

Sponsors and collaborators

Lead sponsor

University of Bari Aldo Moro

Other

Registry information

Official study title

Short Implant Placement for Single-Tooth Rehabilitation in the Atrophic Posterior Maxilla

Important dates

Study start
2014
Primary completion
2024
Study completion
2024
First posted
Jan 6, 2025
Registry last updated
Jan 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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