The aim of this study is to evaluate the effect of flowable conventional and bulk-fill composites on postoperative sensitivity in class I cavities over long-term follow-up. The hypothesis to be tested in this study is that the type of composite material will not affect clinical success.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* good general health
* no heart disease
* no diabetes
* no systemic diseases such as hypertension
Exclusion Criteria:
* Patients with advanced periodontitis and associated postoperative sensitivity,
* Pregnant and breastfeeding women,
* Patients undergoing orthodontic treatment,
* Patients using appliances,
* Patients with direct pulp capping
Primary outcome measure(s)
FDI criteria — 2 years good, very good, poor
Trial sites (1)
Facility
City
Region
Status
Muhammet Karadaş
Merkez
Rize Province
Recruiting
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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