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Caries Prevention Products & Dentinal Hypersensitivity

Primary Purpose

Hypersensitivity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sensodyne
Crest Cavity Protection & MI Paste Plus
Clinpro 5000
Sponsored by
Tufts University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypersensitivity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • At least 18 years of age
  • Tooth with exposed root surface and/or exposed dentin
  • Tooth with a VAS score greater than or equal to 3
  • No adjacent tooth/teeth with sensitivity (as defined as 2 or higher on the VAS)

Exclusion Criteria:

  • Participation in another dental study that may alter the results of this study.
  • A medical condition that could interfere with reliable pain reporting (e.g., pain disorders)
  • Any chronic medical condition that requires the regular use of pain or anti-inflammatory medications
  • Used a desensitizing dentifrice within the preceding four weeks
  • Have received an antihypersensitivity treatment (varnish or precipitating solution) of the identified tooth within the preceding four weeks
  • Undergoing active orthodontic treatment.
  • Teeth with carious lesions, buccal vertical cracks in enamel, evidence of irreversible pulpitis (pain lasting more than five seconds after air stimulation)
  • Pregnant/ lactating patients (Clinpro5000 has 5000ppm fluoride and there is a risk of ingesting the product)
  • Patients with Milk Allergy (CPP-ACP is a dairy based product)
  • Patients on Kidney Dialysis (due to the free calcium in CPP-ACP, dialysis patients should be on a diet with limited calcium)

Sites / Locations

  • Tufts University School of Dental Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Sensodyne

Crest Cavity Protection & MI Paste Plus

Clinpro 5000

Arm Description

There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.

There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.

There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.

Outcomes

Primary Outcome Measures

Dentinal Hypersensitivity
The primary analysis will be to compare the dentinal hypersensitivity between the 3 groups. Air test: A 1 second blast of air from the air-water syringe was applied to the tooth. Water test: Three drops of ice water were be placed on the tooth. Schiff Score Investigator observed participant reaction to test and scored on following scale: 0-Tooth/Subject does not respond to stimulus. Tooth/Subject responds to stimulus, but does not request discontinuation of stimulus. Tooth/Subject responds to stimulus and requests discontinuation or moves from stimulus. Tooth/Subject responds to stimulus, considers stimulus to be painful, and requests discontinuation of the stimulus VAS (visual analog scale): The participant reported sensitivity on a scale of 0-10. 0 being no pain and 10 being worst pain imaginable.

Secondary Outcome Measures

Full Information

First Posted
May 7, 2014
Last Updated
November 17, 2020
Sponsor
Tufts University
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1. Study Identification

Unique Protocol Identification Number
NCT02136576
Brief Title
Caries Prevention Products & Dentinal Hypersensitivity
Official Title
Comparing Three Caries Prevention Products on Dentinal Hypersensitivity - A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
October 2018 (Actual)
Study Completion Date
October 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tufts University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this pilot research project is to compare the clinical effect on dentinal hypersensitivity of three products: Casein Phosphopeptide-Amorphous Calcium Phosphate (CPP-ACP) paste with fluoride, 5000 Sodium Fluoride (NaF) dentifrice containing Tri-Calcium Phosphate (TCP), and a dentifrice containing Potassium Nitrate. The hypothesis of this study is that CPP-ACP with fluoride and 5000ppm NaF with TCP will exhibit a greater reduction in dentinal hypersensitivity compared to the control (dentifrice containing Potassium Nitrate). The results of this pilot study will validate or negate the need for a larger clinical study that may provide generalizable results for using caries-prevention products with the additional benefit of minimizing dentinal hypersensitivity.
Detailed Description
Dentinal hypersensitivity commonly occurs in patients with gingival recession, resulting from a reduced periodontium or in patients who have undergone non-surgical and surgical periodontal therapy (Pradeep 2010, Yilmaz 2011). When the gingiva recede, the root surfaces of the teeth are exposed (West 2008). In addition, after a non-surgical or surgical periodontal procedure, the cementum of the root surface is removed as a result of scaling and root planing. This leaves dentin exposed on the root surface with open dentinal tubules. In addition, dentin is less mineralized than enamel and has a greater susceptibility to and a faster progression of root caries and dentinal hypersensitivity (Saunders 2005). Root caries commonly occurs in patients who have undergone periodontal therapy and extensive root caries often results in the extraction of the tooth (Hull 1997). Dental professionals often make a variety of recommendations to remedy dental hypersensitivity, including the application of fluoride varnishes, anti-hypersensitivity toothpaste, gingival grafting procedures and various restorative procedures, aiming to occlude the dentinal tubules or desensitize the pulpal nerve endings (Brahmbhatt 2012, Orsini 2010). Since the introduction of Caries Management By Risk Assessment (CAMBRA) in the Journal of the California Dental Association in 2007 (Jenson 2007, Young 2007), the marketplace for anti-caries products has surged. As a result, many approaches to the management of dental caries have been introduced and dental practitioners and sales representatives have promoted several anti-caries products. In addition, the reduction or the abatement of the progression of dental caries (coronal, root and interproximal) as a result of a caries management program has been reported (Featherstone 1992, Ito 2012). Many caries management products have ingredients that include fluoride and calcium phosphate (Amorphous Calcium Phosphate-Casein Phosphopeptide (Recaldent ™), (Wang 2012) Tri-Calcium Phosphate ™ or Novamin ™) (Su 2011). Moreover, encouraging clinical findings have been reported, including, but not limited to the reduction of white spot enamel lesions and dentinal hypersensitivity (Kowalczyk 2006). The topical application of "antihypersensitivity" materials is a common recommendation (least invasive of the "standard of care" recommendations) to diminish dentinal hypersensitivity and will serve to provide data for the research study. The study will evaluate which of these products result in the greatest reduction of dentinal hypersensitivity. The application of the experimental products for the reduction of dentinal hypersensitivity is for research purposes. The methods used to test sensitivity in this study have been used in published studies (Brahmbhatt 2012, Holland 1997). The VAS scale used in this study has also been used for tooth sensitivity studies (Holland 1997, Hughes 2010). A 30% decrease in VAS score has been shown to be clinically meaningful (Ritter 2006, Raymond 2008). This pilot study would investigate the ability of anti-caries products to reduce dentinal hypersensitivity when compared to a sensitivity-reducing dentifrice. It would be a novel contribution to the dental community if a material that is proven to reduce tooth decay is also proven to reduce dentinal hypersensitivity. The results may potentially have a tremendous impact on the dental community because it may provide dental professionals a scientifically-supported approach to improve the comfort and quality of life of periodontal patients (patients who are treated for gum disease/ bone loss around teeth) and increase the lifespan of teeth that undergo periodontal treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypersensitivity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sensodyne
Arm Type
Active Comparator
Arm Description
There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.
Arm Title
Crest Cavity Protection & MI Paste Plus
Arm Type
Active Comparator
Arm Description
There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.
Arm Title
Clinpro 5000
Arm Type
Active Comparator
Arm Description
There are no specific characteristics for inclusion in this group. Enrollment will be determined randomly.
Intervention Type
Device
Intervention Name(s)
Sensodyne
Intervention Description
Subjects will be instructed to brush with Sensodyne twice daily (2 minutes each time in the morning and the evening) during the duration of the study.
Intervention Type
Device
Intervention Name(s)
Crest Cavity Protection & MI Paste Plus
Intervention Description
Subjects will be instructed to brush twice daily (2 minutes each time in the morning and the evening) using Crest Cavity Protection toothpaste. They will be instructed to apply MI Paste Plus (CPP-ACP with fluoride) twice daily to the study teeth after brushing their teeth. MI Paste Plus will be applied to the study teeth with a finger.
Intervention Type
Device
Intervention Name(s)
Clinpro 5000
Intervention Description
Subjects will be instructed to brush with Clinpro 5000 twice daily (2 minutes each time in the morning and the evening) during duration of the study.
Primary Outcome Measure Information:
Title
Dentinal Hypersensitivity
Description
The primary analysis will be to compare the dentinal hypersensitivity between the 3 groups. Air test: A 1 second blast of air from the air-water syringe was applied to the tooth. Water test: Three drops of ice water were be placed on the tooth. Schiff Score Investigator observed participant reaction to test and scored on following scale: 0-Tooth/Subject does not respond to stimulus. Tooth/Subject responds to stimulus, but does not request discontinuation of stimulus. Tooth/Subject responds to stimulus and requests discontinuation or moves from stimulus. Tooth/Subject responds to stimulus, considers stimulus to be painful, and requests discontinuation of the stimulus VAS (visual analog scale): The participant reported sensitivity on a scale of 0-10. 0 being no pain and 10 being worst pain imaginable.
Time Frame
8 weeks after baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: At least 18 years of age Tooth with exposed root surface and/or exposed dentin Tooth with a VAS score greater than or equal to 3 No adjacent tooth/teeth with sensitivity (as defined as 2 or higher on the VAS) Exclusion Criteria: Participation in another dental study that may alter the results of this study. A medical condition that could interfere with reliable pain reporting (e.g., pain disorders) Any chronic medical condition that requires the regular use of pain or anti-inflammatory medications Used a desensitizing dentifrice within the preceding four weeks Have received an antihypersensitivity treatment (varnish or precipitating solution) of the identified tooth within the preceding four weeks Undergoing active orthodontic treatment. Teeth with carious lesions, buccal vertical cracks in enamel, evidence of irreversible pulpitis (pain lasting more than five seconds after air stimulation) Pregnant/ lactating patients (Clinpro5000 has 5000ppm fluoride and there is a risk of ingesting the product) Patients with Milk Allergy (CPP-ACP is a dairy based product) Patients on Kidney Dialysis (due to the free calcium in CPP-ACP, dialysis patients should be on a diet with limited calcium)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Britta Magnuson, DMD
Organizational Affiliation
Tufts University School of Dental Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tufts University School of Dental Medicine
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20370417
Citation
Pradeep AR, Sharma A. Comparison of clinical efficacy of a dentifrice containing calcium sodium phosphosilicate to a dentifrice containing potassium nitrate and to a placebo on dentinal hypersensitivity: a randomized clinical trial. J Periodontol. 2010 Aug;81(8):1167-73. doi: 10.1902/jop.2010.100056.
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Results Reference
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18715354
Citation
West NX. Dentine hypersensitivity: preventive and therapeutic approaches to treatment. Periodontol 2000. 2008;48:31-41. doi: 10.1111/j.1600-0757.2008.00262.x. No abstract available.
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Caries Prevention Products & Dentinal Hypersensitivity

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