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Clinical and Radiographic Evaluation of Zirconomer Restorative

Clinical and Radiographic Evaluation of Zirconomer Restorative Material Versus a Glass Ionomer Cement in Restoration of Primary Molars A Randomized Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06254053
Acronym
Zirconomer
Enrollment
24
Registered
2024-02-12
Start date
2024-10-01
Completion date
2025-01-03
Last updated
2024-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries in Children, Dental Materials

Keywords

GIc/Zirconomer

Brief summary

Is zirconomer restorative material more effective than a glass ionomer cement in restoration of primary molars

Detailed description

This trial seeks to evaluate the clinical and radiographic performance of two materials zirconomer restorative material and glass ionomer cement to achieve better treatment for primary molars.

Interventions

Restorative material

OTHERzirconia reinforced glass ionomer

Restorative material

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

statistician

Intervention model description

last decade has seen several innovative additions to enhance the properties of GIC whilst simplifying its usage. Unlike the early glass-ionomers, these newer systems are easy and more practical to use as a dental restorative and luting material for preschoolers, children and teenagers alike. These new varieties are composed of ceramic and zirconia reinforced glass ionomer cements were introduced to provide better drawbacks of amalgam as well as tooth-colored restorative materials exhibiting the strength of amalgam and at the same time maintain the fluoride releasing capacity of GIC providing better mechanical properties.

Eligibility

Sex/Gender
ALL
Age
5 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

* Inclusion criteria: 1. Children having carious primary molars(class1) without pulp exposure and normal radiograph. 2. Children between age 5 and 7 years. 3. Both male and female are included. 4. Cooperative Children.

Exclusion criteria

<!-- --> 1. Patients with systemic diseases. 2. Parent refuse to participate.

Design outcomes

Primary

MeasureTime frameDescription
Recurrent CariesColor match12 MONTHSRadiographic Visual inspection using Modified United States Public Health Service Ryge criteria USPHS

Secondary

MeasureTime frameDescription
Color match12 MONTHSvisual inspection using Modified United States Public Health Service Ryge criteria USPHS
Marginal Discoloration12 MONTHSusing visual inspection Modified United States Public Health Service Ryge criteria USPHS
Marginal Adaptation12 MONTHSusing visual inspection Modified United States Public Health Service Ryge criteria USPHS
-Anatomic Form12 MONTHSusing visual inspection Modified United States Public Health Service Ryge criteria USPHS

Contacts

Primary ContactTamador A hmedIbrahim ali, Master
tamadurah699@gamil.com347-933-7140
Backup ContactMujahed a hmed Ibrahim Ali, MASTER
Mugahed.ali95@gmail.com749-404-6041

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026