Single-session associative protocol for dentin hypersensitivity management: a 1-year randomized, blinded clinical study.

Objectives: This study aimed to establish a single-session associative protocol for non-restorative management of dentin hypersensitivity (DH).

Materials And Methods: Twenty-four individuals with DH and a minimum sensitivity level of 4 on the visual analog scale (VAS) were selected. The study was conducted in a split-mouth design, with each participant ( = 20) having at least 1 affected tooth in all quadrants.