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A Clinical Bite Force Study of Two Marketed Adhesives Against no Adhesive

NCT03037307 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2018-08-31

Study results available
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Summary

The objective of this study will be to compare bite force (BF) measurements over a 12-hour period of a currently marketed denture adhesive cream based on carbomer technology (test), with a positive control and a negative/no treatment control.

Conditions

  • Denture Retention

Interventions

OTHER

Test Product

Five strips of test adhesive cream for upper denture, as per application instructions.

OTHER

Positive Contol

Three dabs of positive control adhesive cream for upper denture, as per application instructions.

OTHER

Negative Control

No adhesive

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-13
Primary Completion
2017-05-04
Completion
2017-05-04

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT03037307 on ClinicalTrials.gov