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Completed

NCT Number: NCT06599320

Variables for Long-term Success in Implant Dentistry

The aims of the present retrospective 25-year study of a sample of 459 patients with 753 sandblasted and acid-etched (SLA) titanium oral implants are:

* to assess the clinical parameters at SLA implants after 25 years in function * to assess the crestal bone levels at SLA implants after 25 years in function * to assess and compare the microbiological conditions at SLA implants and their adjacent teeth after 25 years of function * to assess the periodontal conditions in patients having received SLA implants 25 years ago * to establish a baseline data set for future prospective studies on patients having received SLA implants 25 years ago * to assess the incidence rates of biological, technical, traumatic failures / complications with SLA implants * to assess the incidence rates of technical failures / complications with prosthetic components on SLA implants * to assess the incidence rates of biological, technical, mechanical, esthetic failures / complications with prosthetic reconstructions on SLA implants * to find potential risk factors for biological failures / complications with SLA implants; i.e. patients having lost their teeth due to different reasons (e.g. partial anodontia, caries, periodontitis, endodontic failure, trauma, vertical root fracture), (ii) to calculate the success rates using different thresholds set as success criteria, (iii) to evaluate the influence of medical conditions and tobacco smoking on the long-term prognosis of titanium oral implants, and (iv) to assess the frequency and quality of maintenance * to find potential risk factors for mechanical, technical, esthetic failures/complications with reconstructions seated on SLA implants * to assess the treatment need and utility of implant therapy after 25 years in patients having received SLA implants

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Bern

Bern, Switzerland

About this study

Specific aims

The aims of the present retrospective 25-year study of a sample of 459 patients with 753 sandblasted and acid-etched (SLA) titanium oral implants are:

  • to assess the clinical parameters at SLA implants after 25 years in function
  • to assess the crestal bone levels at SLA implants after 25 years in function
  • to assess and compare the microbiological conditions at SLA implants and their adjacent teeth after 25 years of function
  • to assess the periodontal conditions in patients having received SLA implants 25 years ago
  • to establish a baseline data set for future prospective studies on patients having received SLA implants 25 years ago
  • to assess the incidence rates of biological, technical, traumatic failures / complications with SLA implants
  • to assess the incidence rates of technical failures / complications with prosthetic components on SLA implants
  • to assess the incidence rates of biological, technical, mechanical, esthetic failures / complications with prosthetic reconstructions on SLA implants
  • to find potential risk factors for biological failures / complications with SLA implants; i.e. patients having lost their teeth due to different reasons (e.g. partial anodontia, caries, periodontitis, endodontic failure, trauma, vertical root fracture), (ii) to calculate the success rates using different thresholds set as success criteria, (iii) to evaluate the influence of medical conditions and tobacco smoking on the long-term prognosis of titanium oral implants, and (iv) to assess the frequency and quality of maintenance
  • to find potential risk factors for mechanical, technical, esthetic failures/complications with reconstructions seated on SLA implants
  • to assess the treatment need and utility of implant therapy after 25 years in patients having received SLA implants

Material and methods Out of the pool of patients from the Departments of Oral Surgery and Periodontology and Fixed Prosthodontics at the University of Bern, Switzerland, all patients having received at least one dental implant will be recruited for a comprehensive evaluation 25 years after implant installation and delivery of the reconstruction. The patients had been treated according to a comprehensive treatment strategy prior to the installation of implants and incorporation of reconstructions. All patients were offered maintenance care that was provided either in the School of Dental Medicine, University of Bern, Switzerland, or in the dental practices of the referring dentists at intervals between 3 and 6 months.

All the implants installed were solid screws (SS) with a diameter of 3.3, 4.1 or 4.8 mm, a length between 6-14 mm and a sandblasted and acid-etched surface (SLA) (Straumann® Dental Implant System, Institute Straumann AG, Basel, Switzerland). The implants were placed according to the manufacturer's instructions. The reconstructions were either cemented or screw-retained and consisted of single-unit crowns (SCs) or short-span fixed dental prostheses (FDPs) with or without cantilever extension(s).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

All patients rehabilitated with oral dental implants supporting fixed partial dental prostheses and followed up for at least 20-years.

Exclusion criteria

None

Treatment and study plan

Oral rehabilitation with dental implants

Other

Patients rehabilitated with implant-supported fixed partial dental prostheses

Primary outcomes

  1. Implant survival rate

    Time frame: 25 years

    percentage of implants in-situ

Sponsors and collaborators

Lead sponsor

University of Bern

Other

Registry information

Official study title

Variables for Long-term Success in Implant Dentistry: A Retrospective Cross-sectional Study With a 25 Year Follow-up or More

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 19, 2024
Registry last updated
Jan 23, 2026

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

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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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