Status:

UNKNOWN

DAMP1: The 1T1T Concept Versus Conventional Implant Loading Protocol

Lead Sponsor:

University of Liege

Conditions:

Dental Implant Failure

Dental Prosthesis Failure

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The One tooth - One time (1T1T) innovative approach is a straightforward and cost-effective protocol to replace a missing tooth in the posterior region (Lambert and Mainjot 2017) (see Appendix). The d...

Detailed Description

The present study is designed as a single center comparative controlled trial. This study aims to compare immediate (1T1T) versus delayed loading with a final PICN screw-retained crown (DL-PICN), perf...

Eligibility Criteria

Inclusion

  • Subject must have voluntarily signed the informed consent form before any study related action
  • Age : 18 or above
  • Men/Women
  • Patient in good systemic health (ASA I/ II)
  • No contraindication against oral surgical interventions
  • Full mouth plaque score (FMPI) lower or equal than 25%
  • Patient with two single unit edentulous space in the posterior area, upper or lower jaw, seeking for implant therapy
  • Maximum two missing teeth per quadrant
  • Two single unit edentulous spaces can be contiguous if there are three posterior teeth in occlusal contact in the tested half arch.
  • After the crown placement, at least 3 posterior teeth must be in occlusal contact with the antagonistic teeth in the tested half arch.
  • The tooth at the implant site 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.

Exclusion

  • Autoimmune disease requiring medical treatment
  • Medical conditions requiring prolonged use of steroids
  • Use of Bisphosphonate intravenously or more then ˃ 3 years of oral use
  • 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 (more than 10 cigarettes/day)
  • Prisoners
  • Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance, or unreliability.

Key Trial Info

Start Date :

September 1 2019

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2024

Estimated Enrollment :

28 Patients enrolled

Trial Details

Trial ID

NCT04045574

Start Date

September 1 2019

End Date

September 1 2024

Last Update

August 6 2019

Active Locations (1)

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Institute of Dentistry University of Liege

Liège, Choose A State, Belgium, 4020