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9 risultati
Effectiveness of the Use of Desensitizing Dentifrices Based on Nanocrystals of Hydroxyapatite / 5% Potassium Nitrate / 1450ppm Sodium Monofluorophosphate and Potassium Nitrate 5% / 1426ppm Sodium Floride in the Treatment of Dentine Hypersensitivity. Test Randomized Clinical
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Currently, periodontal treatment, both surgical and non-surgical, leaves sequelae in the vast majority of patients. The loss of clinical insertion level could be an early indicator or a possible risk factor for dentine hypersensitivity (HSD) (15). Therefore, it is necessary to correctly diagnose
Potassium Nitrate and Post-bleaching Sensitivity
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This study will be a randomized, triple-blinded, placebo-controlled clinical trial, and split mouth study design.
The patients included will be submitted to two in-office bleaching sessions receiving the potassium nitrate 5% or placebo gel (prior the bleaching session, for 10 minutes), associated to
Effect of Preoperative Diclofenac Potassium on Postoperative Endodontic Pain
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Patients with moderate-to-severe preoperative pain are selected. Patients receive either a single-dose of 50 mg diclofenac potassium (group A) or a placebo tablet as a control (group B). All patients receive the assigned premedication one hour before single-visit root canal treatment. Postoperative
Clinical and Radiographic Assessments of Potassium Nitrate in Polycarboxylate Versus Mineral Trioxide Aggregate as Pulpotomy Biomaterials in Immature Mandibular First Permanent Molars
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introduction: Vital pulp therapy (VPT) is defined as a treatment which aims to preserve and maintain pulp tissue that has been compromised but not destroyed by caries, trauma, or restorative procedures in a healthy state. Pulpotomy is one of the techniques of VPT where unhealthy pulp in pulp chamber
Diclofenac Potassium on IANB Efficacy in Symptomatic Irreversible Pulpitis
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Objective: The aim of this clinical trial is to evaluate the effect of pre-operative administration of diclofenac potassium on the efficacy of inferior alveolar nerve block on using 2% mepivacaine anaesthetic agent in patients with symptomatic irreversible pulpitis.
Design: Randomized double-blind
Effect of Preoperative Diclofenac Potassium on Articaine Buccal Infitration Success
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This study aims to evaluate the effectiveness of preoperative administration of Diclofenac Potassium (50 mg Cataflam) compared to placebo, one hour before treatment, on the anesthetic success of buccal infiltration with 4% articaine with epinephrine 1:200,000 in mandibular molars with symptomatic
Potassium Oxalate and Placebo and Post-bleaching Sensitivity
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Methods & Materials:
This clinical trial was approved by the Scientific Review Committee and by the Committee for the Protection of Human Subjects of the local University (CAAE 60259916.0.0000.5546).
Trial design:
This study will be a randomized, triple-blinded, placebo-controlled clinical trial,
Potassium Oxalate and Potassium Nitrate and Post-bleaching Sensitivity
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Methods & Materials:
This clinical trial was approved by the Scientific Review Committee and by the Committee for the Protection of Human Subjects of the local university (CAAE 60259316.2.0000.5546).
Trial design:
This study will be a randomized, triple-blinded, placebo-controlled clinical trial,
Use of Biomaterials as Desensitizer Agents
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Participants The study is designed as randomized clinical trial. The participants will be selected from the regular attenders of the Dental Clinic in the University of Sassari, Italy.
Inclusion criteria:
• patients will be considered suitable for the study if they have sensitive teeth showing
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