The trial compares patient-reported postoperative sensitivity of 2 existing dental filling materials. The dental filling materials will be used according to manufacturer's instructions and within the existing CE marked licence. We are interested in investigating which licensed material confers the least postoperative discomfort to our patients in normal clinical use.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
34
2 arm study comparing restoration of a tooth with either FillUp composite or conventional composite
University of Leeds
Leeds, Yorkshire, United Kingdom
RECRUITINGPost operative sensitivity
patient assessment by VAS
Time frame: 1 month
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