NCT07154602

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
6mo left

Started Nov 2025

Status
not yet recruiting

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

Study Progress51%
Nov 2025Nov 2026

First Submitted

Initial submission to the registry

August 25, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

September 4, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

November 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Expected
Last Updated

September 4, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

August 25, 2025

Last Update Submit

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

EXPERIMENTAL

3d printed hybrid ceramic crown for implant prosthesis in anterior and premolars maxillary teeth

Other: 3D printed hybrid resin ceramic crowns

milled hybrid resin ceramic crown

ACTIVE COMPARATOR

milled hybrid resin ceramic crown for implant prosthesis in anterior and premolar maxillary teeth

Other: milled hybrid resin ceramic crown

Interventions

3D printed hybrid resin ceramic crowns in anterior and premolar maxillary teeth

3d printed hybrid ceramic crown

milled hybrid resin ceramic crown on implants in anterior and premolar maxillary teeth

milled hybrid resin ceramic crown

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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