NCT02762201
Terminated
Not Applicable
Clinical Evaluation of Therapeutic Efficiency of Implant-secured Removable Partial Denture: A Randomized, Controlled, Prospective Multicentric Study.
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.
Investigators
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)
Loading locations...
Similar Trials
Recruiting
Not Applicable
Removable Partial Dentures Made of PEEKTooth LossNCT06191107University Hospital Heidelberg50
Completed
Not Applicable
Comparing Cobalt-Chromium Versus PEEK Secondary Telescopic Crowns on Implant Retained Mandibular Overdenture.EdentulismNCT06637930Amr El Sayed Khalifa12
Completed
Not Applicable
Evaluation of Dental Implants After Using Several Bone Splitting TechniquesJaw, EdentulousNCT05720143Damascus University39
Unknown
Not Applicable
The Treatment of Implant-retained Mandibular Overdentures for Edentulous PatientsEdentulousNCT02846805Chufan Ma53
Completed
Not Applicable
Clinical Assessment of All Ceramic Single-retainer Using Upper Canine as Abutment With Minimum Preparation on the Lingual Surface, to Replace the Upper Lateral Incisor and Will be Compared With the All Ceramic Single-retainer Using Upper Central Incisor.Survival, ProsthesisNCT05812066Cairo University54