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3D-printed Endocrowns Versus Prefabricated Zirconia Crowns in Pulpally-treated Primary Molars

NCT04909827 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2023-07-20

No results posted yet for this study

Summary

Aim of the study :

to compare between 3D printed microfilled hybrid composite endocrowns and prefabricated zirconia crowns for restoring pulpally treated primary molars regarding the following aspects: In Vivo aspects Patient satisfaction

\*The esthetic, functional and biological performance according to FDI clinical criteria. At 3, 6 and 12 months

In Vitro aspects:

* Marginal gap.
* Fracture resistance.

Study methodology:

This study is a combined randomized clinical trial and in vitro study .The study will be conducted at the Department of Pediatric Dentistry and Dental Public Health, Faculty of Dentistry,

Ain Shams University as follows:

In vivo comparison of the clinical performance of 3D printed Endocrowns versus prefabricated zirconia crowns regarding esthetic, functional and biological performance according to FDI clinical criteria. In vitro evaluation of the marginal gap and fracture resistance of both types of restorations.

Conditions

  • Pulpotomy
  • Tooth Restoration

Interventions

PROCEDURE

3D-printed endocrown

pulpotomy and restoration with 3D-printed microfilled hybrid composite endocrown

PROCEDURE

Zirconia crown

pulpotomy and restoration with prefabricated zirconia crown

Sponsors & Collaborators

  • Ain Shams University

    lead OTHER

Principal Investigators

  • Mariem O Wassel, PhD · Ainshams university

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
4 Years
Max Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2023-02-28
Completion
2023-02-28

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04909827 on ClinicalTrials.gov