Biodentine® is a most recent material for direct pulp capping. The aim of this study is to
determine the 3 months success rate (defined as clinical and radiographic successes together)
of direct pulp capping realized with Biodentine®.
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Locations near you
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Full eligibility criteria for NCT02891876
Ages eligible for Study
18 Years to 40 Years
Genders eligible for Study
Accepts Healthy Volunteers
adult patients with a small pulp exposure (<2mm) created during decy removal on a vital tooth
absence of spontaneous pain, of fistula, of swelling, of mobility, of periodontal enlargement, of resorption, of periapical pathosis, of furcation defect, on this tooth
normal periodontal probing around this tooth
cold vitality test : positive but non increased on this tooth
patient with at risk of endocarditis,
patient with allergic reactions to a product used in the protocol,
patient with a lack of oral hygiene,
tooth with spontaneous pain, fistula, swelling, increased mobility, periodontal enlargement, resorption, periapical pathosis, furcation defect, pulpal necrosis, pulpal irreversible inflammation, excessive dental destruction, very abundant pulp bleeding, impossible set-up of the rubber dam
tooth with a pulp exposure >2mm
All locations for NCT02891876
Brest, France, 29200
View full eligibility
Tris trial is registered with FDA with number: NCT02891876. The sponsor of the trial is University Hospital, Brest and it is looking for 40 volunteers for the current phase.
Official trial title: 3-months Success Rate of Direct Pulp Capping With Biodentine®
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