Clinical Evaluation of Different Bulk-fill Composite Restorations on Posterior Teeth

NCT ID: NCT06226389

Last Updated: 2024-01-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-17

Study Completion Date

2026-01-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Different bulk-fill composites will be applied in different posterior cavities then compared

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Patients must be in middle age(25-55) age,able to regularly follow up,not pregnant and at least have 4 carious molars

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Carious Teeth

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

4 Different bulk-fill composite

Bulk-fill composite will be applied in different 4 posterior cavities with 3-4 ml in depth

Group Type EXPERIMENTAL

4 different bulk-fill composite

Intervention Type PROCEDURE

Posterior cavities either class 1/2

Aging

For long term follow up

Group Type EXPERIMENTAL

4 different bulk-fill composite

Intervention Type PROCEDURE

Posterior cavities either class 1/2

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

4 different bulk-fill composite

Posterior cavities either class 1/2

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* at least 4 carious molars

Exclusion Criteria

* pregnancy patient
* Not able to regularly follow up
* bad oral hygiene
Minimum Eligible Age

25 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Mansoura University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Asmaa S Elsaeed, Assistant lecturer

Role: PRINCIPAL_INVESTIGATOR

Assistant lecturer

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Mansoura,Faculty of Dentistry

Al Mansurah, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

A02011023

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Comparative Evaluation of Class V Restorations
NCT06164418 ACTIVE_NOT_RECRUITING NA