Dentin Sensitivity
Conditions
Brief summary
Subjects will be enrolled into 3 balanced groups each using a different strength toothpaste. Dental hypersensitivity (DHS) will be assessed at study start, midway and study end.
Detailed description
This study is a double-blind, randomized, placebo-and positive-controlled, stratified parallel group clinical trial. The three groups will be randomly assigned to use one of three test toothpastes having an identical base formulation but containing respectively either 0% nano-hydroxyapatite (HAP) (placebo), 15% nano-HAP or 5% KNO3 (positive control). All dental examinations for data collection will be conducted by the same Clinical Examiner.
Interventions
OTHERPlacebo
0% nano-HAP toothpaste
DEVICE15% nano-HAP toothpaste
Toothpaste with identical base formulation as the placebo containing 15% nano-HAP
DEVICE5% KNO3 toothpaste
Toothpaste with identical base formulation as the placebo containing 5% KNO3
Sponsors
Sangi Co., Ltd.
The University of Texas Health Science Center at San Antonio
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
* Males or females between the age of 20 and 80 years, of any socio-economic status * Diagnosed as having DHS, i.e. having at least one sensitive tooth with demonstrated cervical erosion/abrasion or gingival recession * Showing a sensitivity response to both tactile and cold air stimulus delivered by a Yeaple probe and a one-second blast of cold air respectively * Patients must be reliable, cooperative and of adequate intelligence to read and understand the rating scales and other study instructions * Patients must be able to read, comprehend, and sign the informed consent form * The teeth and sites to be tested should be on the buccal/labial surfaces of incisors, canines, premolars or molars where the affected sites are accessible * Teeth selected for testing should have a plaque index of ≤ 2
Exclusion criteria
* The sensitive tooth is associated with concomitant oral pain due to any other condition such as soft-tissue lesions, tooth-ache ascribable to dental caries, tooth fracture, or cracked tooth syndrome, or pain due to other surgical procedures or injuries. * The sensitive tooth is associated with a periodontal abscess as diagnosed from an X-ray or clinical examination of the tooth * The sensitive tooth is associated with mobility \>1 * The sensitive tooth is associated with gum pain from gingivitis, occlusal trauma, thermal or chemical burns * Patients having pain from periodontal-related causes but not DHS * Previous professional desensitizing treatment * Patients using medication which could interfere with the perception of pain * Medical histories marked by chronic use of anti-inflammatory agents, daily analgesics, anticonvulsants, antihistamines, antidepressants, sedatives and/or other psychotropic drugs * Pregnancy or breastfeeding * Allergies and idiosyncratic responses to toothpaste ingredients * Eating disorders or conditions associated with vomiting * Systemic conditions that are etiologic or predisposing to DHS * Excessive dietary or environmental exposure to acids * The sensitive tooth was restored in the preceding three months * The sensitive tooth is an abutment tooth for fixed or removable prostheses * The sensitive tooth has extensive restoration or restorations extending into the test area * Patients below 20 years or above 80 years of age * Smokers
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measurement of Cold Air Stimulus | Week 0 (baseline), 4 weeks and 8 weeks | The primary efficacy outcome will be the decrease in cold air stimulus sensitivity (VAS score) from baseline to 8 weeks. Assessment of change in cold air sensitivity will be conducted using air delivered from a standard dental unit air syringe at room temperature (\ 70°F±3°F)(\ 21°C±2°C) and a pressure of 60psi (± 5psi). Assessment of sensitivity will be carried out using Visual Analog Scale (VAS). Tooth sensitivity was measured using a Cold Air Stimulus. When being assessed, participants rated their perception of the pain/discomfort experienced when cold air was directed at the exposed root of each tooth by marking a single vertical line on a Visual Analogue Scale (VAS) scale from 0 to 100 mm, where 0 = No Pain/Discomfort and 100 = Intense Pain/Discomfort. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Measurement of Tactile Stimulus | Week 0 (baseline), 4 weeks and 8 weeks | The secondary efficacy outcome will be the increase in tactile stimulus force from baseline to 8 weeks. Assessment of Change in tactile sensitivity will be assessed using the Yeaple Electronic Force Sensing Probe.The explorer tip will be applied perpendicular to the tooth surface and a pressure load applied starting at 10 g and increasing to 80g. The load at which the subject says yes will be recorded. (Baseline screening will begin at 30g). |
Countries
United States
Participant flow
Recruitment details
Subjects were consented and enrolled, then for one month there was a washout period. Baseline characteristic measurements were taken prior to washout for both Cold Air Sensitivity and Tactile Stimulus.
Participants by arm
| Arm | Count |
|---|---|
| Toothpaste 1 Toothpaste 1 containing 0% nano-hydroxyapatite (HAP) will be used by subjects to brush their teeth twice daily for 3 minutes in the morning and before bed each night using a 1 inch strip of toothpaste on a soft-bristled toothbrush.
Placebo: 0% nano-HAP toothpaste | 62 |
| Toothpaste 2 Toothpaste 2 containing 15% nano-HAP will be used by subjects to brush their teeth twice daily for 3 minutes in the morning and before bed each night using a 1 inch strip of toothpaste on a soft-bristled toothbrush.
15% nano-HAP toothpaste: Toothpaste with identical base formulation as the placebo containing 15% nano-HAP | 59 |
| Toothpaste 3 Toothpaste 3 containing 5% potassium nitrate (KNO3) will be used by subjects to brush their teeth twice daily for 3 minutes in the morning and before bed each night using a 1 inch strip of toothpaste on a soft-bristled toothbrush.
5% KNO3 toothpaste: Toothpaste with identical base formulation as the placebo containing 5% KNO3 | 62 |
| Total | 183 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Treatment Period | Lost to Follow-up | 2 | 5 | 0 |
| Treatment Period | Physician Decision | 0 | 0 | 2 |
Baseline characteristics
| Characteristic | Toothpaste 1 | Toothpaste 2 | Toothpaste 3 | Total |
|---|---|---|---|---|
| Age, Continuous | 47 years STANDARD_DEVIATION 16 | 47 years STANDARD_DEVIATION 16 | 50 years STANDARD_DEVIATION 14 | 48 years STANDARD_DEVIATION 15 |
| Cold Air Sensitivity (VAS) | 69 units on a scale STANDARD_DEVIATION 20 | 67 units on a scale STANDARD_DEVIATION 16 | 65 units on a scale STANDARD_DEVIATION 18 | 67 units on a scale STANDARD_DEVIATION 18 |
| Race/Ethnicity, Customized Asian | 15 Participants | 4 Participants | 12 Participants | 31 Participants |
| Race/Ethnicity, Customized Black (not Hispanic) | 3 Participants | 2 Participants | 1 Participants | 6 Participants |
| Race/Ethnicity, Customized Hispanic | 30 Participants | 28 Participants | 26 Participants | 84 Participants |
| Race/Ethnicity, Customized White (not Hispanic) | 14 Participants | 25 Participants | 23 Participants | 62 Participants |
| Region of Enrollment United States | 62 participants | 59 participants | 62 participants | 183 participants |
| Sex: Female, Male Female | 44 Participants | 43 Participants | 43 Participants | 130 Participants |
| Sex: Female, Male Male | 18 Participants | 16 Participants | 19 Participants | 53 Participants |
| Tactile (g) | 15 grams STANDARD_DEVIATION 7 | 15 grams STANDARD_DEVIATION 7 | 16 grams STANDARD_DEVIATION 7 | 15.3 grams STANDARD_DEVIATION 7 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 64 | 0 / 64 | 0 / 64 |
| other Total, other adverse events | 0 / 64 | 0 / 64 | 0 / 64 |
| serious Total, serious adverse events | 0 / 64 | 0 / 64 | 0 / 64 |
Outcome results
Primary
Measurement of Cold Air Stimulus
The primary efficacy outcome will be the decrease in cold air stimulus sensitivity (VAS score) from baseline to 8 weeks. Assessment of change in cold air sensitivity will be conducted using air delivered from a standard dental unit air syringe at room temperature (\ 70°F±3°F)(\ 21°C±2°C) and a pressure of 60psi (± 5psi). Assessment of sensitivity will be carried out using Visual Analog Scale (VAS). Tooth sensitivity was measured using a Cold Air Stimulus. When being assessed, participants rated their perception of the pain/discomfort experienced when cold air was directed at the exposed root of each tooth by marking a single vertical line on a Visual Analogue Scale (VAS) scale from 0 to 100 mm, where 0 = No Pain/Discomfort and 100 = Intense Pain/Discomfort.
Time frame: Week 0 (baseline), 4 weeks and 8 weeks
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Toothpaste 1 | Measurement of Cold Air Stimulus | Week 4 | 51.1 units on a scale | Standard Deviation 1.84 |
| Toothpaste 1 | Measurement of Cold Air Stimulus | Week 8 | 35.6 units on a scale | Standard Deviation 1.9 |
| Toothpaste 1 | Measurement of Cold Air Stimulus | Week 0 (Baseline) | 71.4 units on a scale | Standard Deviation 1.4 |
| Toothpaste 2 | Measurement of Cold Air Stimulus | Week 8 | 37.7 units on a scale | Standard Deviation 2.19 |
| Toothpaste 2 | Measurement of Cold Air Stimulus | Week 0 (Baseline) | 72.2 units on a scale | Standard Deviation 1.47 |
| Toothpaste 2 | Measurement of Cold Air Stimulus | Week 4 | 51.9 units on a scale | Standard Deviation 2.28 |
| Toothpaste 3 | Measurement of Cold Air Stimulus | Week 4 | 62 units on a scale | Standard Deviation 2 |
| Toothpaste 3 | Measurement of Cold Air Stimulus | Week 0 (Baseline) | 71.9 units on a scale | Standard Deviation 1.61 |
| Toothpaste 3 | Measurement of Cold Air Stimulus | Week 8 | 48.4 units on a scale | Standard Deviation 2.21 |
Secondary
Measurement of Tactile Stimulus
The secondary efficacy outcome will be the increase in tactile stimulus force from baseline to 8 weeks. Assessment of Change in tactile sensitivity will be assessed using the Yeaple Electronic Force Sensing Probe.The explorer tip will be applied perpendicular to the tooth surface and a pressure load applied starting at 10 g and increasing to 80g. The load at which the subject says yes will be recorded. (Baseline screening will begin at 30g).
Time frame: Week 0 (baseline), 4 weeks and 8 weeks
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Toothpaste 1 | Measurement of Tactile Stimulus | 4 Weeks | 23.6 Grams | Standard Deviation 1.15 |
| Toothpaste 1 | Measurement of Tactile Stimulus | 0 weeks (Baseline) | 13.7 Grams | Standard Deviation 0.48 |
| Toothpaste 1 | Measurement of Tactile Stimulus | 8 weeks | 31.7 Grams | Standard Deviation 1.58 |
| Toothpaste 2 | Measurement of Tactile Stimulus | 4 Weeks | 23.2 Grams | Standard Deviation 1.37 |
| Toothpaste 2 | Measurement of Tactile Stimulus | 0 weeks (Baseline) | 14.1 Grams | Standard Deviation 0.57 |
| Toothpaste 2 | Measurement of Tactile Stimulus | 8 weeks | 28.7 Grams | Standard Deviation 1.77 |
| Toothpaste 3 | Measurement of Tactile Stimulus | 0 weeks (Baseline) | 14.8 Grams | Standard Deviation 0.57 |
| Toothpaste 3 | Measurement of Tactile Stimulus | 8 weeks | 22.9 Grams | Standard Deviation 1.27 |
| Toothpaste 3 | Measurement of Tactile Stimulus | 4 Weeks | 17.7 Grams | Standard Deviation 1.06 |