Esthetic Outcome of 3D Printed Hybrid Ceramics as Final Restorations for Single Screw Retained Implant.
NCT ID: NCT07154602
Last Updated: 2025-09-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
32 participants
INTERVENTIONAL
2025-11-01
2026-11-01
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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3d printed hybrid ceramic crown
3d printed hybrid ceramic crown for implant prosthesis in anterior and premolars maxillary teeth
3D printed hybrid resin ceramic crowns
3D printed hybrid resin ceramic crowns in anterior and premolar maxillary teeth
milled hybrid resin ceramic crown
milled hybrid resin ceramic crown for implant prosthesis in anterior and premolar maxillary teeth
milled hybrid resin ceramic crown
milled hybrid resin ceramic crown on implants in anterior and premolar maxillary teeth
Interventions
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3D printed hybrid resin ceramic crowns
3D printed hybrid resin ceramic crowns in anterior and premolar maxillary teeth
milled hybrid resin ceramic crown
milled hybrid resin ceramic crown on implants in anterior and premolar maxillary teeth
Eligibility Criteria
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Inclusion Criteria
* 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
* 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).
18 Years
70 Years
ALL
No
Sponsors
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International Dental Contiuing Education
NETWORK
Responsible Party
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Ingy Ghobrial Kastour
Dr.Ingy Kastour
Central Contacts
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Nourhan Gamal Dr.Nourhan Gamal AbdEl-Aziz, Master holder
Role: CONTACT
Other Identifiers
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IDCE-12208025
Identifier Type: -
Identifier Source: org_study_id
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