Skip to main content
Clinical Trials/NCT05766878
NCT05766878
Completed
N/A

The Rehabilitation of Atrophic Jaws Using Short Implants With Different Surface Characteristics: Multicentric RCT

University of Foggia3 sites in 1 country30 target enrollmentJune 9, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peri-Implantation Loss
Sponsor
University of Foggia
Enrollment
30
Locations
3
Primary Endpoint
Marginal Bone remodeling around the implant
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of the research is to evaluate the clinical outcome of short dental implants, characterized by a new macro-structural design and inserted in the upper or lower jaw in patients with reduced bone volume. The clinical outcomes will be compared for different surface treatments of implant neck and those of prosthetic components.

Registry
clinicaltrials.gov
Start Date
June 9, 2023
End Date
February 17, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Foggia
Responsible Party
Principal Investigator
Principal Investigator

Khrystyna Zhurakivska

Researcher

University of Foggia

Eligibility Criteria

Inclusion Criteria

  • healthy patients, with edentulous maxillary or mandibular ridge, requiring rehabilitation with two adjacent implants;
  • at least 6 month after extraction;

Exclusion Criteria

  • post-extractive implants;
  • sites requiring bone regeneration or maxillary sinus lift;
  • general health problems that contraindicate implant treatment.

Outcomes

Primary Outcomes

Marginal Bone remodeling around the implant

Time Frame: 0-4-12 months after implant placement

The marginal bone remodeling will be evaluated by Radiographic examination. Periapical radiographs will be performed using paralleling technique with a Rinn-type positioner, customized for each patient at implant placement (T0), prosthetic restoration delivery (T1), and after 12 months (T2).Peri-implant bone levels will be measured at each time point as the linear distance (in mm) between implant platform and bone crest at mesial and distal aspects of each implant. A positive value will be assigned if the bone crest is coronal to the implant platform, whereas a negative value will be assigned if the first bone-to implant contact is apical to the implant platform. All measurements will be performed by two examiners, using measuring software (Image J). Each measurement will be performed three times at three different points.

Secondary Outcomes

  • Periodontal indexes: Probing Depth(The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.)
  • Implant Stability evaluation(0-4 months.)
  • Suppuration on probing(The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.)
  • Bleeding on Probing(The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.)
  • Plaque index of peri-implant tissues(The measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.)

Study Sites (3)

Loading locations...

Similar Trials