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Completed

NCT Number: NCT06709508

Retrospective Evaluation of Prosthetic Complications and Peri-implant Bone Resorption in Implant-supported Single Unit Fixed Restorations

This study evaluated the one-year outcomes of implant-supported single-tooth fixed restorations used to replace missing teeth. The aim was to assess the success rates of dental implants and identify potential complications during treatment. A total of 100 individuals aged between 20 and 64 participated in the study. Patients were evaluated one year after their implant treatments through clinical examinations and radiographic imaging.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Afyonkarahisar University of Health Sciences Faculty of Dentistry, Department of Prosthodontics

Afyonkarahisar, Turkey (Türkiye)

About this study

Aim: The aim of this study was to retrospectively investigate the prosthetic complications and peri-implant bone loss by clinical and radiological examination at the 12th month of implantsupported single-unit fixed restorations.

Materials and Methods: In this retrospective study, 100 volunteer patients, aged between 20 and 64, who received implant-supported single-member fixed restoration treatment, were scanned from the archives and included. The patients were scanned from the archives, called for 12-month follow-ups, and clinical and radiographic evaluations were made. G*Power (G*Power Ver. 3.0.10, Franz Faul, Üniversität Kiel, Germany) package program was used to calculate the sample size. Digital radiographs (periapical-panoramic films) taken from the patients at the end of the implant treatment and at the 12th month follow-up were recorded using Planmeca Romexis® software. ImageJ, a digital image analysis program, was used to evaluate marginal bone loss on radiographs (ImageJ 1.54g- Wayne Rasband and Contributons, National institutes of Health, USA). In evaluating the success and survival of the implants, the criteria in the consensus decisions published at the International Oral Implantology Congress in 2007 were taken as basis. In addition, prosthetic complications such as chipping, screw loosening and decementation; Its relationship with anatomical localization, implant length, implant diameter, abutment type, superstructure material, occlusal table and the condition of the opposing arch was evaluated.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Participants were required to be over 18
  • Not to have any systemic disorders
  • Not to smoke
  • Have provided consent to the study.

Exclusion criteria

  • Individuals with any systemic or psychiatric disorders
  • Who did not have radiographic data immediately after prosthetic loading

Treatment and study plan

Examination group

Other

This study differs from other clinical studies because the participants of this study consisted of patients undergoing single-member implant-supported restoration treatment at the Department of Prosthodontics, Afyonkarahisar Health Sciences University.

Primary outcomes

  1. Implant survival rate

    Time frame: 12 months

  2. Prosthetic complication rate

    Time frame: 12 months

    This study evaluated the impact of various parameters, including abutment type, occlusal table width, and opposing arch condition, on prosthetic complications such as debonding (descementation), screw loosening, and chipping (porcelain fractures).

Sponsors and collaborators

Lead sponsor

Özer İşisağ

Other

Registry information

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Nov 29, 2024
Registry last updated
Nov 29, 2024

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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