Three-Year Clinical Performance of Fiber-reinforced Versus Indirect Resin Composite Posterior Restorations
NCT ID: NCT06803537
Last Updated: 2025-05-11
Study Results
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.
ACTIVE_NOT_RECRUITING
NA
33 participants
INTERVENTIONAL
2022-01-01
2025-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Clinical Performance of Two Fiber Reinforced Resin Composites Versus Nanohybrid Resin Composite in Posterior Teeth Will be Evaluated Using Modified USPHS Criteria
NCT05380973
Clinical Performance of Short Fiber Reinforced Flowable Resin Composite Restorations 2y RCT
NCT04720638
Clinical Performance of Fiber Reinforced Composite Versus Microhybrid Composite Restorations
NCT03515265
Comparing Between Two Different Restoration
NCT05556551
One-year Clinical Evaluation of Bulk-fill Versus Conventional Incremental Posterior Restoration by FDI Criteria
NCT02891967
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Fiber-reinforced composite
indirect lab composite
indirect lab processed resin composite inlay restorations
Conventional resin composite
conventional microhybrid resin composite posterior restorations
Indirect lab composite
Fiber-reinforced composite
short fiber-reinforced composite used as base covered by conventional composite
Conventional resin composite
conventional microhybrid resin composite posterior restorations
Conventional microhybrid resin composite
Fiber-reinforced composite
short fiber-reinforced composite used as base covered by conventional composite
indirect lab composite
indirect lab processed resin composite inlay restorations
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Fiber-reinforced composite
short fiber-reinforced composite used as base covered by conventional composite
indirect lab composite
indirect lab processed resin composite inlay restorations
Conventional resin composite
conventional microhybrid resin composite posterior restorations
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Good oral hygiene: patients with low and moderate caries risk (according to Caries management by caries risk assessment CAMBRA sheets) were enrolled in this study.
3. The visual examination should reveal the presence of a minimum of three primary occlusal or proximal caries (Black Class I and II) with a severity score of 4 or 5 according to the International Caries Detection and Assessment System (ICDAS).
4. The carious teeth must exhibit vitality and do not display periapical radiolucency as evaluated by periapical radiography.
5. The selected teeth must be under stable occlusion.
Exclusion Criteria
2. Extremely poor oral hygiene
3. Chronic periodontitis
4. Heavy bruxism
5. Cavities with a buccolingual width exceeding two-thirds of the intercuspal distance or requiring cusp covering.
6. Patients undergoing orthodontic procedures.
7. Patients unable to attend the scheduled recall appointments.
20 Years
35 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mansoura University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mansoura university
Al Mansurah, Dakahlia Governorate, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
A02071221
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.