Clinical Evaluation of Implant-secured Removable Partial Denture

Not Applicable

Terminated

• Conditions: Tooth Loss

• Registration Number: NCT02762201
• Lead Sponsor: Hospices Civils de Lyon

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-05-16
• Study First Submitted: 2016-05-03
• Study First Submitted QC: 2016-05-03
• Study First Posted: 2016-05-04
• Primary Completion: 2019-06-06
• Study Completion: 2019-06-06
• Status Verified: 2019-08
• Last Update Submitted: 2019-08-22
• Last Update Posted: 2019-08-28

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 13

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
prosthetic success rate	5 years after prosthesis delivery

Secondary Outcome Measures

Name	Time	Method
prosthetic success rate	6 months, 1 year, 2 years, 3 years and 4 years after prosthesis delivery

Trial Locations

Locations (1)

Hospices Civils de Lyon; 🇫🇷 Lyon, France