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Clinical Trials/NCT02762201
NCT02762201
Terminated
Not Applicable

Clinical Evaluation of Therapeutic Efficiency of Implant-secured Removable Partial Denture: A Randomized, Controlled, Prospective Multicentric Study.

Hospices Civils de Lyon1 site in 1 country13 target enrollmentMay 16, 2014
ConditionsTooth Loss

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth Loss
Sponsor
Hospices Civils de Lyon
Enrollment
13
Locations
1
Primary Endpoint
prosthetic success rate
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

This study aims to compare the therapeutic efficiency of implant-secured removable partial denture (PASI) with the therapeutic efficiency of the metalic standard removable partial denture (PAC) in the treatment of intermediate extended-gap (4 adjacent teeth). The therapeutic efficiency will be assessed by the 5 years-prosthetic success rate.

Registry
clinicaltrials.gov
Start Date
May 16, 2014
End Date
June 6, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with at least a 4 to 6 adjacent teeth intermediate extended-gap (excluding wisdom teeth) in the upper or lower jaw.
  • Patients with at least 4 conservable teeth by dental arch, without major occlusal trouble.
  • Patients with healthy periodontium, allowing metalic standard removable partial denture delivery : bleeding on periodontal probing for a duration less than 30 seconds, Osteolysis of the alveolar ridge less or equal to 50%, attachment loss less or equal to 5mm
  • Patients with a sufficient bone volume for implant placement, without prior bone supply.

Exclusion Criteria

  • Patients with general counter-indications for implant placement.
  • Patients suffering from a titanium allergy.
  • Patients with an insufficient oral and dental hygiene - Patients smoking ten or more cigarettes per day.
  • Patients with teeth extended-gap, which could be corrected by a fixed tooth-supported denture.
  • Patient with an insufficient available bite level to deliver an attachment system (\< 7mm).
  • Patients with a severe generalized chronic periodontitis , an aggressive periodontitis or a periodontitis unresponsive to treatment.
  • Women who have reported to be pregnant.
  • Patients deprived of liberty

Outcomes

Primary Outcomes

prosthetic success rate

Time Frame: 5 years after prosthesis delivery

Secondary Outcomes

  • prosthetic success rate(6 months, 1 year, 2 years, 3 years and 4 years after prosthesis delivery)

Study Sites (1)

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