Esthetic Outcome of 3D Printed Hybrid Ceramics as Final Restorations for Single Screw Retained Implant.
1 other identifier
interventional
32
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2025
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 25, 2025
CompletedFirst Posted
Study publicly available on registry
September 4, 2025
CompletedStudy Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2026
ExpectedSeptember 4, 2025
August 1, 2025
3 months
August 25, 2025
August 26, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Aesthetic appearance
using visual analogue scale, patient rating from 0 to 10 where 10 is satisfied the most while 0 is least satisfied
6 months
Secondary Outcomes (1)
Prosthetic complications
6 months
Study Arms (2)
3d printed hybrid ceramic crown
EXPERIMENTAL3d printed hybrid ceramic crown for implant prosthesis in anterior and premolars maxillary teeth
milled hybrid resin ceramic crown
ACTIVE COMPARATORmilled hybrid resin ceramic crown for implant prosthesis in anterior and premolar maxillary teeth
Interventions
3D printed hybrid resin ceramic crowns in anterior and premolar maxillary teeth
milled hybrid resin ceramic crown on implants in anterior and premolar maxillary teeth
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Nourhan Gamal Dr.Nourhan Gamal AbdEl-Aziz, Master holder
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- NETWORK
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.Ingy Kastour
Study Record Dates
First Submitted
August 25, 2025
First Posted
September 4, 2025
Study Start
November 1, 2025
Primary Completion
February 1, 2026
Study Completion (Estimated)
November 1, 2026
Last Updated
September 4, 2025
Record last verified: 2025-08