MedTrace Logo

A Clinical Study to Evaluate the Maximum Maxillary Bite Force (BF) When Using Two Novel Denture Adhesives Compared to Using No-Adhesive

NCT05173974 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-02-16

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to investigate the hold properties of two experimental denture adhesives using established maximum incisal BF methodology.

Conditions

  • Denture Retention

Interventions

DEVICE

Super Poligrip Free

A single application of 1 gram of Super Poligrip Free will be applied topically to oral tissues via the upper denture.

DEVICE

Experimental Denture Adhesive 1

A single application of 1 gram of Experimental Denture Adhesive 1 will be applied topically to oral tissues via the upper denture.

DEVICE

Experimental Denture Adhesive 2

A single application of 1 gram of Experimental Denture Adhesive 2 will be applied topically to oral tissues via the upper denture.

Sponsors & Collaborators

  • HALEON

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2022-02-08
Primary Completion
2022-07-12
Completion
2022-07-12
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT05173974 on ClinicalTrials.gov