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Partial Rehabilitation Using a PEEK-acrylic Resin Removable Partial Denture

NCT05589506 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-08-21

No results posted yet for this study

Summary

The goal of this observational study is to evaluate the outcome of a Poly-ether-ether-ketone - acrylic resin removable partial denture used in partial edentulous rehabilitation after one year of follow-up. The main question it aims to answer is:

\- What is the survival outcome of partial rehabilitations using Poly-ether-ether-ketone-acrylic resin removable partial dentures? The participants will receive a definitive removable partial denture incorporating Poly-ether-ehter-ketone.

Conditions

  • Prosthesis Survival

Interventions

DEVICE

Removable partial denture PEEK

A removable partial denture incorporating PEEK and acrylic resin in its composition used as definitive prosthesis to rehabilitate partial edentulism in the maxilla or mandible.

Sponsors & Collaborators

  • Invibio Ltd

    collaborator INDUSTRY

  • Malo Clinic

    lead OTHER

Principal Investigators

  • Miguel A de Araújo Nobre, PhD · Director of Research, Development and Education

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-13
Primary Completion
2025-03-31
Completion
2025-03-31

Countries

  • Portugal

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05589506 on ClinicalTrials.gov