Status:

COMPLETED

Benefit of the Digital Workflow for Screw-retained Single Implant Restorations

Lead Sponsor:

University of Liege

Conditions:

Tooth Loss

Eligibility:

All Genders

Phase:

PHASE4

Brief Summary

The aim of this research project is emphasize the benefit of the digital workflow compared to conventional impressions and crown processing with standard la procedures. The objectives of the present s...

Eligibility Criteria

Inclusion

  • Subject must have voluntarily signed the informed consent form before any study related action
  • Age: 18 with one or more missing teeth in the maxillary area, seeking for implant therapy.
  • Men/Women
  • In good systemic health (ASA I/ II)
  • Present with no contra indication against oral surgical interventions
  • Patients required replacement of a single missing tooth. The tooth at the implant site(s) must have been extracted or lost at least 12 weeks before the date of implantation.
  • At least 10 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

  • Autoimmune disease require medical treatment
  • Medical conditions requiring prolonged use of steroids
  • Use of Bisphosphonate intravenously or more then
  • Infection (local or systemic) - patient with gingivitis or active local infection will undergo a medical treatment prior to his entrance to the study, each individual will be evaluated prior to study procedure for suitability, in case of systemic infection the evaluation will be based on medical anamneses, and if necessary will be referred to relevant medical tests.
  • Current pregnancy or breastfeeding women
  • Alcoholism or chronically drug abuse
  • Immunocompromised patients
  • Uncontrolled Diabetes
  • Smokers
  • Prisoners

Key Trial Info

Start Date :

January 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2017

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT03234868

Start Date

January 1 2016

End Date

June 1 2017

Last Update

July 31 2017

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