Clinical Trials Directory

Trials / Terminated

TerminatedNCT02762201

Clinical Evaluation of Implant-secured Removable Partial Denture

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

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Hospices Civils de Lyon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREPASIImplant-secured removable partial denture will be delivered in 2 large steps: implant delivery followed by denture delivery. * Implant delivery will take 4 dental consultations : a pre-implant study at Day14 after inclusion, the surgical implant insertion at D28 after inclusion, stitches removal at D35 after inclusion, and finally functional implant delivery between 3 or 6 month after surgery (to allow implant osteointegration). * Denture delivery will take 6 weekly dental consultations between Week 3 and Week 8 after the functional implant delivery.
PROCEDUREPACMetalic standard removable partial denture, the standard treatment, will be delivered in 4 steps at Day 7, D14, D21, D28 after inclusion, as classically.

Timeline

Start date
2014-05-16
Primary completion
2019-06-06
Completion
2019-06-06
First posted
2016-05-04
Last updated
2019-08-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02762201. Inclusion in this directory is not an endorsement.