Clinical Performance of Zirconia Reinforced GI Versus Conventional Viscous GI in Geriatric Patients

Phase 2

Completed

• Conditions: Performance; Geriatric
• Interventions: Drug: Ketac Molar quick Aplicap; Drug: Zirconomer Improved

• Registration Number: NCT04298151
• Lead Sponsor: Cairo University

Brief Summary

This study is conducted to evaluate the clinical performance of Zirconomer Improved GI restoration compared to Conventional viscous GI restoration in geriatric patients with Posterior carious lesions in class I or II cavities

Detailed Description

This study will be conducted to determine the clinical performance of the Zirconia reinforced glass ionomer restorations ( Zirconomer improved) under stress bearing posterior area (class I or claa II cavities) in geriatric population in comparison to Conventional viscous glass ionomer restorations (Ketac molar quick Aplicap) using the modified United States Public Health Service (USPHS) criteria

P: Geriatric Patients with posterior Caries lesions I: Zirconia reinforced GI (Zirconomer Improved) C: Conventional viscous GI, (Ketac Molar quick Aplicap) O: The Clinical performance of the Glass Ionomer restorations Using USPHS Criteria

Study Timeline

• Study First Submitted: 2020-03-04
• Study First Submitted QC: 2020-03-04
• Study First Posted: 2020-03-06
• Study Start: 2021-09-01
• Primary Completion: 2022-09-01
• Study Completion: 2022-10-01
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-05
• Last Update Posted: 2024-02-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

• Age range 60-80 years
• Geriatric patients with Class I or II Posterior carious lesions.
• Males or Females.
• Pulp asymptomatic vital carious posterior teeth.
• Co-operative patients approving to participate in the trial.

Exclusion Criteria

• Age range less than 60 years.
• Disabilities.
• Deep extensive carious cavities that may lead to fracture of the tooth or pulpal affection.
• Teeth with signs and symptoms of irreversible pulpitis or pulp necrosis.
• Heavy smoking.
• Lack of compliance.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
ketac molar quick aplicap	Ketac Molar quick Aplicap	conventional viscous glass ionomer restoration
zirconomer improved	Zirconomer Improved	zirconia reinforced glass ionomer restoration

Primary Outcome Measures

Name	Time	Method
Clinical performance	1 year	clinical performance of the Glass Ionomer restorations using modified USPHS criteria

Trial Locations

Locations (1)

Doaa Abdou; 🇪🇬 Giza, Egypt