BridgeMD
New treatment option for Jaw, Edentulous, Partially
Official title Two-unit Cantilever Implant Prostheses Made of Monolithic Zirconia or PFM
ClinicalTrials.gov ID: NCT04713800
What this study is testing
- What it's testing
- The aim of is to compare the survival rate and technical outcomes of cantilever implant-supported fixed denture prosthetics (cFDPs) made either out of monolithic zirconia bonded to a titanium base in a digital workflow, or porcelain fused-to metal using a gold abutment in a conventional workflow. In addition, biological outcomes, wear patterns, PROMs and time efficiency will be recorded.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 22 and older. Healthy volunteers may be eligible.
You may be able to join if
- Minimal age of 22 years old.
- No general medical condition which represents a contraindication to implant treatment
- Good oral hygiene (PII ≤ 20%), and healthy periodontal tissues (BOP≤ 20%)
- Two adjacent-teeth gap in posterior maxilla or mandible arch (first premolar, second premolar, first molar, second molar) with an osseointegrated...
- Presence of antagonist occlusal units
You likely can't join if
- Severe bruxism or clenching habits
- Patients with inadequate oral hygiene or persistent intraoral infection
- Women who are pregnant or breast feeding at the day of inclusion
- Smokers exceeding 15 cigarettes / day, or equivalent; patients chewing tobacco
- Unable or unwilling to cooperate for the trial period
- Estimated cantilever crown mesial-distal length \> 10 mm
See the full eligibility criteria
- Minimal age of 22 years old.
- No general medical condition which represents a contraindication to implant treatment
- Good oral hygiene (PII ≤ 20%), and healthy periodontal tissues (BOP≤ 20%)
- Two adjacent-teeth gap in posterior maxilla or mandible arch (first premolar, second premolar, first molar, second molar) with an osseointegrated regular or wide-diameter bone-level implant in a prosthetically correct...
- Presence of antagonist occlusal units
- Severe bruxism or clenching habits
- Patients with inadequate oral hygiene or persistent intraoral infection
- Women who are pregnant or breast feeding at the day of inclusion
- Smokers exceeding 15 cigarettes / day, or equivalent; patients chewing tobacco
- Unable or unwilling to cooperate for the trial period
- Estimated cantilever crown mesial-distal length \> 10 mm
- Estimated implant crown height (from implant platform to occlusal contact points) \> 15 mm
The study team makes the final eligibility decision.
Where it's taking place
- Geneva, Switzerland
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, 22 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Geneva, Switzerland. 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.