A Clinical Study to Compare Professional Treatments for Dentinal Hypersensitivity

Procter & Gamble (P&G)

Status

Completed

Conditions

Dentinal Hypersensitivity

Treatments

Device: Super Seal® Desensitizer

Device: Acclean® Fluoride Varnish

Study type

Interventional

Funder types

Industry

Identifiers

NCT03405259

2013077

Details and patient eligibility

About

The objective of this study is to compare professional treatments for dentinal hypersensitivity immediately following a single, professionally-applied treatment and again approximately 2 months following treatment.

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

be at least 18 years of age;
provide written informed consent prior to participation and be given a signed copy of the informed consent form;
be in good general health as determined by the Investigator/designee; and
have at least one tooth with a VAS score of greater than or equal to 30 in response to the air challenge.

Exclusion criteria

allergy to rosin or to pine nuts;
self-reported pregnancy or nursing;
severe periodontal disease, as characterized by purulent exudate, generalized mobility, and/or severe recession;
active treatment for periodontitis;
fixed facial orthodontic appliances;
any diseases or conditions that might interfere with the safe completion of the study; or
an inability to undergo any study procedures.