Actively Recruiting
A Study to Assess the Effectiveness of a Marketed Denture Adhesive in Real-World Setting
Led by HALEON · Updated on 2026-04-21
375
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this decentralised study in a real-world setting is to assess the effectiveness of a marketed denture adhesive (Poligrip Power Max Hold + Seal) in preventing food entrapment under dentures (self-assessed). The study will evaluate participants perceived food occlusion of a marketed denture adhesive over three weeks compared to no adhesive use over three weeks in a real-world setting.
CONDITIONS
Official Title
A Study to Assess the Effectiveness of a Marketed Denture Adhesive in Real-World Setting
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant has signed informed consent before any assessments
- Participants of any gender
- Participants aged 18 years or older at screening
- Willing and able to follow all study procedures and restrictions
- In good general and mental health with no significant medical or oral conditions impacting safety or study outcomes
- Habitual wearer of partial or full dentures for most waking hours
- Self-assessed relatively well-fitted dentures
- Resides in the United States excluding Hawaii and Alaska
You will not qualify if you...
- Employees involved in the study or their immediate families, including those of Lindus Health or Haleon
- Participation in other investigational studies within 30 days before or during this study
- Previous enrollment in this study
- Recent or current treatment for periodontal or gum disease within 6 months
- Diagnosed active periodontitis, candida infection, or active tooth decay
- Chronic or severe painful conditions requiring frequent pain medication use
- Significant oral abnormalities affecting study participation
- Acute or chronic medical or psychiatric conditions affecting safety or study integrity
- Diagnosed xerostomia or medications causing dry mouth
- Known intolerance or allergy to study materials or ingredients
- History of alcohol or substance abuse within the past year
- History of swallowing difficulties or choking
- Any denture adjustments or treatments altering fit during the study
- Current or prior use of bisphosphonate drugs
- Planned surgery during the study period
- Inability to read and understand English
- Investigator's judgment deeming participant unsuitable for the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Lindus Health (virtual site)
Boston, Massachusetts, United States, 02111
Actively Recruiting
Research Team
H
Haleon Response Center
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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