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A Clinical Study to Compare Professional Treatments for Dentinal Hypersensitivity

Procter & Gamble (P&G) logo

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

22 participants in 2 patient groups

Super Seal® Desensitizer
Experimental group
Description:
Professionally Applied
Treatment:
Device: Super Seal® Desensitizer
Acclean® Fluoride Varnish
Sham Comparator group
Description:
Professionally Applied
Treatment:
Device: Acclean® Fluoride Varnish

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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