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A Study to Measure the Efficacy of a Toothpaste on Dentinal Hypersensitivity

NCT03244618 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 272

Last updated 2020-10-05

Study results available
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Summary

Double blind parallel study to measure the efficacy of a toothpaste containing calcium-silicate/phosphate on dentinal hypersensitivity compared to a control toothpaste containing fluoride

Conditions

  • Dentin Sensitivity

Interventions

DEVICE

CSSP Toothpaste

Toothpaste containing calcium silicate, sodium phosphate and sodium monofluorophosphate

DEVICE

Fluoride Toothpaste

Toothpaste containing sodium monofluorphosphate

Sponsors & Collaborators

  • University of Bristol

    collaborator OTHER

  • Unilever R&D

    lead INDUSTRY

Principal Investigators

  • Nicola X West, Professor · University of Bristol

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-06-19
Primary Completion
2018-06-13
Completion
2018-06-13

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03244618 on ClinicalTrials.gov