BridgeMD
New treatment option for Prosthesis User
Official title Clinical Performance of 3D-Printed Resin and Zirconia Implant Restorations
ClinicalTrials.gov ID: NCT07522671
What this study is testing
- What it's testing
- This randomized controlled clinical trial evaluates the clinical performance of 3D-printed resin restorations compared with milled monolithic zirconia in implant-supported single crowns and short-span fixed partial dentures (FPDs). A total of patients requiring one or two implant-supported restorations in the mandibular anterior region were randomly allocated to receive either 3D-printed permanent resin restorations (CROWNTEC) or conventionally milled zirconia prostheses.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 60
You may be able to join if
- Participants must meet all of the following:
- Age ≥18 years.
- Have one or two osseointegrated dental implants requiring prosthetic restoration.
- Demonstrate stable peri-implant tissues with no signs of inflammation or implant mobility.
- Maintain good oral hygiene and controlled periodontal status.
You likely can't join if
- Participants are excluded if they have any of the following:
- Severe parafunctional habits (e.g., bruxism).
- Uncontrolled systemic diseases affecting bone metabolism or healing.
- Peri-implantitis or compromised implant stability.
- Requirement for cantilever prostheses or long-span restorations, or FPDs in areas other than the mandibular anterior region.
See the full eligibility criteria
- Participants must meet all of the following:
- Age ≥18 years.
- Have one or two osseointegrated dental implants requiring prosthetic restoration.
- Demonstrate stable peri-implant tissues with no signs of inflammation or implant mobility.
- Maintain good oral hygiene and controlled periodontal status.
- Require either:
- A single implant-supported crown, or
- A short-span (maximum 3-unit) implant-supported fixed partial denture (FPD) supported by two implants in the mandibular anterior region.
- Participants are excluded if they have any of the following:
- Severe parafunctional habits (e.g., bruxism).
- Uncontrolled systemic diseases affecting bone metabolism or healing.
- Peri-implantitis or compromised implant stability.
- Requirement for cantilever prostheses or long-span restorations, or FPDs in areas other than the mandibular anterior region.
The study team makes the final eligibility decision.
Where it's taking place
- Shibīn al Kawm, Egypt
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, 18 years to 60 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Shibīn al Kawm, Egypt. 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.