Actively Recruiting
A Study Evaluating Oral-Health-Related Quality of Life and Treatment Patterns Among Dentin Hypersensitivity Sufferers
Led by HALEON · Updated on 2026-04-28
375
Participants Needed
1
Research Sites
58 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary purpose of this study is to characterize changes in Oral-Health-Related Quality of Life (OHrQoL), as measured by the Dentin Hypersensitivity Experience Questionnaire (DHEQ) over a 12-month period.
CONDITIONS
Official Title
A Study Evaluating Oral-Health-Related Quality of Life and Treatment Patterns Among Dentin Hypersensitivity Sufferers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant who has provided consent indicating they have been informed of all pertinent aspects of the study.
- All genders who, at the time of screening, are aged 18 years or older.
- Anyone who has begun to experience dentin hypersensitivity (self-reported) within the past three months.
- Anyone who has started to use products to treat their tooth sensitivity within the past three months.
- Participant who is able to independently complete all activities online.
- Participants residing in the United States.
You will not qualify if you...
- Anyone who has any chronic health conditions that could impact their participation in this study, such as cancer, mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period.
- Participant whose sensitivity could be caused by other factors or clinical pathology than dentin hypersensitivity, including tooth cavities, significant gum disease, cracked or fractured teeth, temporomandibular joint disease, or recent tooth extractions or fillings within the last three months.
- Anyone who wears braces or Invisalign-like appliances for treatment or dentures (full or partial).
- Participant who has undergone treatment for periodontal or gum disease within 6 months of screening or is currently undergoing treatment for periodontal or gum disease.
- Participant who has been informed by a dental health care professional that they have active periodontitis.
- Participant who has been informed by a dental health care professional that they have active caries.
- Participant with any chronic or severe painful health condition(s) requiring regular use of pain relief medications more than 3 days a week.
- Anyone who has participated in another dentin hypersensitivity study within the last three months.
- Currently participating in or planning to participate in any other research study during this study's duration.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Citruslabs (Virtual Site)
Las Vegas, Nevada, United States, 89118
Actively Recruiting
Research Team
H
Haleon Response Center
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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