3M(TM) Filtek(TM) Supreme Flowable Composites for Class IV and Veneers (NCT07128589) | Clinical Trial Compass
RecruitingNot Applicable
3M(TM) Filtek(TM) Supreme Flowable Composites for Class IV and Veneers
United States75 participantsStarted 2025-08-07
Plain-language summary
This clinical study aims to evaluate the clinical performance of 3M™ Filtek™ Supreme Flowable Composite in class IV and veneer indication. Follow-ups of 7 days, 6, 12, and 24 months will be conducted following an Fédération Dentaire Internationale (FDI) modified score (2023). A minimum of 50 Class IV and 25 veneers will be included in the evaluation. Research data and pictures will be provided for each patient pre-op and at 7 days (baseline, 6 months, 12 months and 24 months. Evaluation will be conducted by two calibrated evaluators different from the operator according to FDI clinical criteria.
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age between 18 -75 years old
* must be willing and able to provide informed consent to participate in the study
* must be available for the required post-operative follow-up study visits
* must be in good general health
* must be in good oral health hygiene (FMPS \< 20%)
* have at least 6 anterior maxillary teeth
* Central and lateral incisors with class IV or Veneer indications. Veneers will be performed exclusively with its contralateral teeth (pairs).
Exclusion Criteria:
* Single tooth veneers
* Canines
* Periodontal disease
* Pulpal diseases
* Occlusal dysfunctions (end-to-end bite)
* Lack of occlusal stability
* Missing posterior teeth, affecting the occlusal distribution
* Study tooth, adjacent tooth, or opposing tooth with mobility \> grade 2 using the Miller's tooth mobility index
* Systemic or local disorders that contra-indicate the dental procedures needed in this study
* Rampant, uncontrolled caries
* Heavy use of smoking tobacco (1 pack or equivalent a day) or chewing tobacco
* Evidence of xerostomia
* Evidence of severe bruxing or clenching, or in need of Temporomandibular Joint (TMJ) related therapy
* Known allergic reaction and/or sensitivity to research materials being used
* Condition or history of chronic use of anti-inflammatory, analgesic (pain), and/or mind altering drugs for medical (including psychiatric) and pharmacotherapeutic therapies that might alter the perception of pain
* Tooth surface loss (attrition, erosion, abrasion…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.