Polyoxymethylene (POM) in the Production of Telescopic Denture in Older Adults With Subtotal Edentulism

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65-100
SponsorUniversity of Belgrade

About this trial

The mail goal of this study is to evaluate the success of the prosthetic treatment with telescopic removable partial denture with framework made of polyoxymethylene (POM). In accordance with the growing older population, who often require complex dental care, it is very important to test simple yet effective and safe solutions. Bearing in mind that POM has proven to be a good solution for conventional removable partial dentures with clasps (RPD), and that it is quite common to have 2-3 remaining teeth, a denture with a framework made of light and flexible material such as POM present a good solution. The hypothesis is that a POM telescopic denture is clinically as adequate, effective and safe as the conventional complex cobalt chromium molybdenum alloy denture with clasps. Telescopic denture should provide better comfort and longevity compared to conventional RPD because of axial loading of the abutment teeth and no negative biological effect of clasps. Moreover, conventional telescopic denture is made of precious alloys which increase their cost; therefore, POM telescopic denture present great advantage in cost/effective treatment. Telescopic crowns are comprised of inner and outer crowns; accordingly, telescopic denture represent a type of complex denture where one part is fixed on the remaining teeth (inner crowns) and other part (outer crowns and denture framework) is removable.

The key factors that will define the success of the treatment will be: assessment of dentures' retention, oral health related quality of life, presence of biological complications, presence of mechanical complications, denture appearance and chewing function assessment.

Eligibility criteria

Qualifiers

patients aged 65 and over

patients with subtotal edentulism

patients who sign an informed consent for participation in the study

retention teeth must have a minimum crown/root ratio of 1:1

Disqualifiers

patients younger than 65 years

patients with temporomandibular joint dysfunction

patiens with bruxism

presence of intrabony defects around the retention teeth

Trial design

Treatments tested in this trial

  • Production of polyoxymethylene telescopic denture
  • Production of conventional complex partial denture with clasps

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators