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Clinical Performance of Onlay Restorations After Cervical Margin Relocation (CMR)

NCT06155773 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2023-12-08

No results posted yet for this study

Summary

The current study intends to evaluate the effect of cervical margin relocation with different restorative materials on three-year clinical performance of indirect Computer-Aided-Design (CAD)/ Computer-Aided-Manufacture (CAM) onlay restorations. This study is designed to test the null hypothesis that the three-year clinical performance of onlay restorations is significantly affected by cervical margin relocation with different restorative materials.

Conditions

  • Dental Caries

Interventions

PROCEDURE

Highly viscous glass ionomer (cervical margin relocation)

different dental restorative materials used to relocate deep cervical margins before receiving onlay restorations

PROCEDURE

Low shrinkage Flowable Composite (cervical margin relocation)

different dental restorative materials used to relocate deep cervical margins before receiving onlay restorations

PROCEDURE

Resin Modified Glass Ionomer (cervical margin relocation)

different dental restorative materials used to relocate deep cervical margins before receiving onlay restorations

PROCEDURE

Bioactive Ionic Resin (cervical margin relocation)

different dental restorative materials used to relocate deep cervical margins before receiving onlay restorations

Sponsors & Collaborators

  • Mansoura University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-24
Primary Completion
2022-01-05
Completion
2025-01-31

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 NCT06155773 on ClinicalTrials.gov