At a glance
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A Prospective, Randomized, Clinical Trial Comparing the Efficacy of Sensi-IP Toothpaste With a Sodium Fluoride Toothpaste in the Treatment of Dentinal Hypersensitivity
In Brief
A clinical study evaluating Sensi-IP toothpaste and Sodium Fluoride Toothpaste for Dentinal Hypersensitivity. Completed, enrolled 46 participants across 1 site.
Detailed Summary
The study is designed as a prospective, randomized, parallel arm, double blinded, pilot clinical trial.The primary objective is to evaluate the efficacy of Sensi-IP +NaF as compared to a NaF toothpaste in the reduction of dentin hypersensitivity in adult participants over 14 days. Study endpoints include Evaporative Air blast Stimuli (Schiff Airblast Sensitivity Score), Tactile Stimuli (Yeaple probe Assessment), Visual Analogue Scale Evaporative Stimuli and the occurrence of adverse events. The study will include 2 study arms: 1. Sodium fluoride toothpaste with Sensi IP (N=23) and 2. Sodium fluoride toothpaste (N=23). Total of 46 participants (ages 18-80 years) with at least one hypersensitive tooth in 2 different quadrants which are anterior to the molars will be enrolled.
Study Details
Timeline
Interventions
Brushing daily with the Sensi-IP toothpaste for 14 days for dentinal hypersensitivity.
Brushing daily with the Sodium Fluoride toothpaste for 14 days for dentinal hypersensitivity.