Recruiting NA Subtotal Edentulism

New treatment option for Subtotal Edentulism

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

ClinicalTrials.gov ID: NCT06593925

What this study is testing

What it's testing
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.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 65 to 100. Healthy volunteers may be eligible.

You may be able to join if

  • 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
  • retention teeth must have sufficient tooth substance (at least two walls)

You likely can't join if

  • patients younger than 65 years
  • patients with temporomandibular joint dysfunction
  • patiens with bruxism
  • presence of intrabony defects around the retention teeth
  • presence of pathological tooth mobility
  • presence of periapical inflammatory processes, abscesses and fistulas in the region of retention teeth
See the full eligibility criteria
Who can join
  • 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
  • retention teeth must have sufficient tooth substance (at least two walls)
What rules you out
  • patients younger than 65 years
  • patients with temporomandibular joint dysfunction
  • patiens with bruxism
  • presence of intrabony defects around the retention teeth
  • presence of pathological tooth mobility
  • presence of periapical inflammatory processes, abscesses and fistulas in the region of retention teeth
  • presence of fetor and suppuration from periodontal pockets of retention teeth

The study team makes the final eligibility decision.

Where it's taking place

  • Belgrade, Serbia

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65 years to 100 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Belgrade, Serbia. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.