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Clinical Trials/NCT02898311
NCT02898311
Unknown
Not Applicable

One-Tooth One-Time (1T1T) A Straightforward Approach to Replace Missing Teeth in the Posterior Region: a Case Series

University of Liege2 sites in 1 countryJuly 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Implant Failed
Sponsor
University of Liege
Locations
2
Primary Endpoint
Prosthesis complication rate
Last Updated
6 years ago

Overview

Brief Summary

This study evaluates the success rate, as the biological and prosthesis complications, of posterior single-unit implants immediately loaded with a chair side Computer-Aided Design and Manufacturing (CAD-CAM) composite crown, after a follow-up period of 6 months,1,2,3,4 and 5 years.

Complementary ex vivo analyses will be performed to evaluate the wear of restorations. The time and cost benefit of the presented digital workflow, as patient centered outcomes will also be evaluated.

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
September 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mainjot Amélie

Associate professor- Head of Clinic

University of Liege

Eligibility Criteria

Inclusion Criteria

  • 0 In good systemic health (ASA I/ II)
  • Present with no contra indication against oral surgical interventions
  • The tooth at the implant site(s) must have been extracted or lost at least 12 weeks before the date of implantation.
  • At least 8 mm of bone in the vertical dimension
  • At least 6 mm of bone in the bucco-lingual dimension.
  • No need for bone augmentation procedure in any of the dimensions
  • Full mouth plaque score (FMPI) lower or equal than 25%
  • Exclusion Criteria
  • Autoimmune disease requiring medical treatment
  • Medical conditions requiring prolonged use of steroids

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Prosthesis complication rate

Time Frame: 6 months

Implant complication rate

Time Frame: 6 months

Secondary Outcomes

  • Evaluation of treatment duration, timing (in minutes) all the different steps of the surgical and prosthodontic procedure.(1 day)
  • Evaluation of patient satisfaction with VAS (visual analog scale) questionnaire(6 months)

Study Sites (2)

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