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Dental fillings rated by patients: immediate vs. One-Week satisfaction

NCT ID NCT07174271

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study looked at how satisfied 50 adults were with their front-tooth composite (tooth-colored) fillings right after the procedure and again one week later. Patients rated the fillings on appearance, smoothness, gum health, and sensitivity using a simple 0-10 scale. The goal was to see if their opinions changed over time and to better understand what matters most to patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

50 people

The number who actually took part.

Started

Jun 2023

Finished

Jun 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population will consist of systemically healthy individuals aged 18 to 35 years who are capable of understanding and providing informed consent. Eligible participants must present with clinically healthy gingiva and periodontium, no bleeding or plaque accumulation, and vital maxillary incisors and canines (teeth 11, 12, 13, 21, 22, 23) without signs of irreversible pulpitis. Individuals with systemic diseases, disabilities, poor oral hygiene compliance, contraindications to rubber dam placement (e.g., asthma, mouth breathing, partially erupted or malposed teeth, latex allergy), or with signs of periapical or pulpal pathology will be excluded.

Ages

18 to 35 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 18-35 years old * Sufficient cognitive ability to understand the consent process * Clinically healthy gingiva and periodontium * No bleeding or plaque accumulation * Vital upper incisors and canines without signs of irreversible pulpitis (11-12-13-21-22-23) Exclusion Criteria: * Any disability (mental health conditions, mental disabilities and physical disabilities) * Systemic diseases or serious medical risks (cardiovascular disorders, diabetes, hypertension, epilepsy) * Compliance problems, inability to maintain hygiene after treatment * Patients contraindicated for rubber dam placement (patient with asthma diagnosis, mouth breathing, partially erupted teeth, excessively malposed teeth and latex allergy) * Signs of periapical pathology or pulpal posterior or anterior pathology

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Conditions

The condition(s) this trial relates to.

Patient Satisfaction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Marmara University Faculty of Dentistry

    Istanbul, Istanbul Asya Kitasi, 34846, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.