Esthetic Outcome of 3D Printed Hybrid Ceramics as Final Restorations for Single Screw Retained Implant.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: 3D printed hybrid resin ceramic crowns, milled hybrid resin ceramic crown.
- Who it may be relevant to
- Registry conditions: 3D Printing. Basic parameters: 18 years — 70 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Esthetic Outcome of 3D Printed Hybrid Ceramics as Final Restorations for Single Screw Retained Implant. A Clinical Randomized Clinical Trial
Overview
clinical trial The goal of this clinical trial is to record the esthetic outcome of the 3d printed hybrid resin crowns. It will also test which method of fabrication is advantageous than the other one. The main questions it aims to answer are: Does any of the fabrication methods differ in its esthetic outcome? Researcher will compare 3d printing fabrication to conventional fabrication method which is the milling technique to see if 3d printing of hybrid resin serves patients a better crown's esthetic outcome. Participants will: Receive a crown after implants are osseointegrated Visit the clinic once every 3 months for checkups and tests Keep records of level of patient's satisfaction.
Interventions
- Other 3D printed hybrid resin ceramic crowns
3D printed hybrid resin ceramic crowns in anterior and premolar maxillary teeth - Other milled hybrid resin ceramic crown
milled hybrid resin ceramic crown on implants in anterior and premolar maxillary teeth
Primary outcome measures
- Aesthetic appearance [Time frame: 6 months]
Secondary outcome measures (1)
- Prosthetic complications [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- Age: between 18 and 70 years old at the time of screening.
- Patients with implants placed and in need for crown restoration
- Medically free with no systemic diseases.
- Good oral hygiene with no active periodontal disease.
- Patient's having adequate interocclusal and mesiodistal restorative space for the fabrication of a single implant-supported crown.
- Patients willing and able to provide written informed consent for participation in the study, understanding its risks, benefits, and alternative treatments.
Exclusion criteria
- Uncontrolled systemic diseases (e.g., uncontrolled diabetes, severe cardiovascular disease, active autoimmune disorders, uncontrolled thyroid dysfunction).
- Patients with composite restoration on the labial/buccal surface implant's neighbouring.
- Immunocompromised patients or those undergoing immunosuppressive therapy.
- Patients undergoing radiation therapy to the head and neck region, or chemotherapy.
- Patients currently on or with a history of medications known to significantly affect bone metabolism (e.g., long-term bisphosphonates, corticosteroids).
- Pregnancy or lactation.
- Known allergies to titanium, resin components, or any other materials used in the study (e.g., composite, zirconia).
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07154602 · IDCE-12208025