Evaluation of the Effect of Flowable Composites on Postoperative Sensitivity in Class I Restorations.
NCT ID: NCT07343050
Last Updated: 2026-01-15
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.
RECRUITING
120 participants
OBSERVATIONAL
2025-05-16
2027-08-01
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.
Evaluation of the Clinical Performance of Different Composite Materials in Class III and IV Restorations.
NCT07343063
Clinical Comparison of Composite Materials
NCT06058026
A 24-month Clinical Evaluation of Different Bulk-fill Restorative Resins in Class II Restorations
NCT03527953
Clinical Comparison of Restorative Materials
NCT06637605
Clinical Evaluation of a Bioactive Material
NCT04825379
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.
CASE_CONTROL
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Dental restorations
Composite restorations
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* no heart disease
* no diabetes
* no systemic diseases such as hypertension
Exclusion Criteria
* Pregnant and breastfeeding women,
* Patients undergoing orthodontic treatment,
* Patients using appliances,
* Patients with direct pulp capping
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Recep Tayyip Erdogan University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Muhammet Karadaş
Clinical Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Elanur Yıldızoğlu, Dr
Role: PRINCIPAL_INVESTIGATOR
Recep Tayyip Erdogan University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Muhammet Karadaş
Merkez, Rize Province, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RTEUDHFMKARADAS005
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.