Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Enrolling by invitation Phase 4

Evaluate the Efficacy of an Oral Health Behavioral Intervention in People With Diabetes

NCT07619729 · tracked via the Priya Life Science USA tracker
Phase
Phase 4
Started
2026-05-26
Last updated
2026-09-03

Condition(s) studied

Diabetes Type 2Periodontal DiseaseCaries

Investigational drug(s) / intervention(s)

Diabetes Oral Health ProgramStannous Fluoride Dentifrice →Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash

Diabetes Oral Health Program: All subjects will receive a behavioral intervention through text messages with links to educational pages about oral health or diabetes. Subjects will have the option of selecting in to the product intervention.

Stannous Fluoride Dentifrice: This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.

Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash: This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.

Study summary

The purpose of this clinical study is to evaluate the effect of a behavioral intervention on the number of preventive and treatment dental claims in a population of people with Type 2 Diabetes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Consented to participation in the Fidelis Care Diabetes Care program. * Aged 18 years and older * English speaking. * Willing and able to receive text messages, and participate in online activities for the duration of the program. * Diagnosis of Type 2 Diabetes. Exclusion Criteria: * Severe cognitive impairment. * General anesthesia in the past 3 months. * Type 1 diabetes. * Self-reported pregnant.

Primary outcome measure(s)

  • Dental Claims — 12 months
    Percentage of preventive dental claims compared to treatment dental claims

Trial sites (1)

FacilityCityRegionStatus
Decentralized Site - Virtual/Remote (NY, USA) Long Island City New York

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07619729 on ClinicalTrials.gov ↗ ← All trials in the USA