The General Aim is to Implement Clinical Assessment of Overload by Voluntary Bite Force Registration to Enable Future Simple But Precise Risk Assessment to Provide Individualized Treatment Plans.

NCT07266701 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 85

Last updated 2025-12-05

No results posted yet for this study

Summary

The general aim of this clinical trial is to implement clinical assessment of overload by bite force registration to enable future simple but precise risk assessment to provide individualized treatment plans.

The main questions it aims to answer are:

* Can we risk-assess patients regarding overload based on bite force measurement before dental implant treatment?
* Can we profile patients based on bite force to tailor precise dental implant treatment for individual patients?
* Will this profiling lead to improved prognosis by reduced number of technical and/or biological complications?

Participants with dental implant prostheses get their bite force measured and followed every year up to 10 years to see complications.

Conditions

  • Dental Implant
  • Bruxism
  • Bite Force
  • Dental Prosthesis Complication
  • Overload

Interventions

DIAGNOSTIC_TEST

Bite force device. Innobyte Kube Innovation TM

The study is not really an intervention

RADIATION

dental radiology

It is a routine modality to take xray to se implant connection and marginal bone level.

Sponsors & Collaborators

  • Smile Tandvård

    collaborator UNKNOWN
  • Malmö University

    lead OTHER

Principal Investigators

  • Tom Bergengren · Malmö University Dental school

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-15
Primary Completion
2026-05-15
Completion
2035-05-15

Countries

  • Sweden

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07266701 on ClinicalTrials.gov