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Hema Free Versus Hema Containing Adhesives in Posterior Restorations

NCT06612021 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2024-09-25

No results posted yet for this study

Summary

The aim of study is to evaluate the clinical performance of posterior restorations using HEMA free universal adhesive versus HEMA containing universal adhesive over one year using USPHS criteria.

Conditions

  • Dental Caries

Interventions

PROCEDURE

Beautibond universal adhesive

HEMA free universal adhesive

PROCEDURE

Tetric N universal bond

HEMA containing universal bond

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Alaa F Abdelsalam, phD · lecturer of conservative dentistry, Cairo university

  • Hadier M Gad, PhD · Lecturer of conservative dentistry, Cairo university

  • Manar A Elmokanen, PhD · Lecturer of conservative dentistry, Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-07-14
Primary Completion
2024-10-14
Completion
2024-11-01

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 NCT06612021 on ClinicalTrials.gov