Intra Oral Kinetics of Fluoride Containing Dentifrices

Tooth Erosion Clinical Trial

Official title:

Intra-oral Kinetics of Fluoride Containing Dentifrices in a Modified Saliva Clearance Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02548156
• Other study ID #: 204777
• Status: Completed
• Phase: N/A
• First received: September 10, 2015
• Last updated: January 16, 2017
• Start date: September 2015
• Est. completion date: October 2015

Study information

• Verified date: January 2017
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to assess the impact of formulation differences on fluoride retention clearance with US levels of fluoride (1150 ppm of fluoride) by evaluating and comparing between treatments the concentrations of fluoride and calcium ions in saliva over 60 minutes after a single brushing with US marketed fluoridated dentifrices and following a dietary acid challenge post 60 minutes of brushing with study treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 29
• Est. completion date: October 2015
• Est. primary completion date: October 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Demonstrates understanding of the study procedures, restrictions and willingness to participate as evidenced by voluntary written informed consent and has received a signed and dated copy of the informed consent form

• Aged 18-65 years

• Understands and is willing, able and likely to comply with all study procedures and restrictions

• Good general and mental health with, in the opinion of the investigator or medically qualified designee:

1. No clinically significant and relevant abnormalities of medical history or oral examination

2. Absence of any condition that would impact on the participant's safety or well being or affect the individual's ability to understand and follow study procedures and requirements

• A minimum of 20 permanent natural teeth

• A gum-base stimulated whole saliva flow rate = 0.8 mL/min and an unstimulated whole saliva flow rate = 0.5 mL/min.

Exclusion Criteria:

• Pregnant or breast feeding women

• Presence of chronic debilitating disease.

• Any condition that causes xerostomia as determined by the Investigator.

• Evidence of untreated caries.

• Gross periodontal disease.

• Tongue or lip piercing or presence of dental implants. Professional tooth cleaning or dental treatment during study. Oral surgery or extraction within 6 weeks of the screening visit.

• Self reported oral symptoms including lesions, sores or inflammation

• Known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients

• Currently taking antibiotics or have taken antibiotics within 2 weeks of the screening visit

• Any medication that could affect salivary flow or cause xerostomia as determined by the Investigator

• Use of multivitamins, calcium supplements and or fluoride supplements within 7 days of treatment phase

• Participant unwilling to abstain from smoking for at least 4 hours on the day of each test visit

• Recent history (within the last year) of alcohol or other substance abuse.

Related Conditions & MeSH terms

• Tooth Erosion

Intervention

Other:
• Test Dentifrice
Marketed dentifrice containing 1150ppm fluoride and 5% w/w KNO3
• Reference Dentifrice
Marketed dentifrice containing 1150ppm fluoride and 5% w/w KNO3
• Comparator Dentifrice
Marketed dentifrice containing 1150ppm fluoride and 5% w/w KNO3
• Orange Juice
Teeth will be rinsed with orange juice followed by rinsing with de-ionised water in test dentifrice and comparator dentifrice arms.
• De-ionised water
Teeth will be rinsed with de-ionised water followed by reference dentifrice and followed by rinsing with orange juice in test dentifrice and comparator dentifrice arms.

Locations

Country	Name	City	State
United Kingdom	GSK Investigational Site	Ellesmere Port	Cheshire

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Concentrations of Fluoride Ions in Saliva 60 Minutes Post Brushing Prior to Administration of the Orange Juice or De-ionised Water Rinse	Concentration of fluoride ions in saliva at 60 minutes after a single brushing with a fluoride dentifrice prior to rinsing with either de-ionised (DI) water or orange juice (OJ). Descriptive data is presented as least square (LS) mean and standard error (SE). SE for Fluoride is the SE of the raw mean.	60 minutes
Secondary	Concentrations of Fluoride and Calcium Ions in Saliva Post Brushing Prior to Administration of Orange Juice or De-ionised Water Rinse	Concentration of fluoride and calcium ions in saliva at baseline, 1, 5, 10, 15, 30 and 60 minutes (for calcium only) after a single brushing with a fluoride dentifrice	up to 60 minutes
Secondary	Concentrations of Fluoride and Calcium Ions in Saliva Following Administration of the Orange Juice or De-ionised Water Rinse	Concentration of fluoride and calcium ions in saliva following a rinse with either de ionised water or OJ 60 minutes after a single brushing with a fluoride dentifrice	60 minutes
Secondary	Concentrations of Fluoride and Calcium Ions in the Initial Expectorate, De-ionised Water Rinse Post Brushing Expectorate, and 60 Minutes Post Brushing Following Administration of Orange Juice or De-ionised Water Rinse	Concentration of fluoride and calcium ions in the initial expectorate, de-ionized water rinse post brushing expectorate, and 60 minutes post brushing following administration of orange juice or de-ionised water rinse	up to 60 minutes