Dentin Hypersensitivity Clinical Trial
Official title:
Salivary Levels of Fluoride and Silver 7 Days After Treatment With Diammine Silver Fluoride
The aim of the study is to measure salivary fluoride and silver levels up to 7 days
post-treatment.
The participants will be 6 healthy adults. They will be given a fluoride free toothpaste to
use the day before the study and all during the study.
3 participants will have 6 teeth treated (Group A).3 participants will have 28 teeth treated
each on the facial aspect (Group B).
On day 0, the participant will be given 25 ml of de-ionized fluoride free water to swish in
the mouth and spit the entire contents into a 50 ml collection tube. This will be done 3
times.
On day 0, 10 minutes after the rinsing and spitting, the participant will provide a
unstimulated salivary sample into a universal collection tube until 5 ml are collected. The
tubes with saliva will be stored on ice and then frozen at -20oC for transfer to the lab at
the University of Washington.
On Day 0, Isolation and application of silver fluoride.
The quadrant will be isolated with cotton rolls, and surrounding gingiva will be covered with
petroleum jelly to provide additional protection.
After application, participant will be given 25 ml of fluoride free water to rinse as in 1
above and water collected. This will be done 10 times.
DAY 1-6 Salivary Collection
Measures: Fluoride will be measured using standard fluoride electrode analysis (Martinez-Mier
et al., 2011). Silver will be measured using Inductively Coupled Plasma-Mass Spectrometry
(EPA 6020a Rev.1 2007) at the University of Washington
Aim: to measure salivary fluoride and silver levels up to 7 days post-treatment. Based on
extrapolation of the study by Vasquez and colleagues (2012), it is hypothesized that 7-day
levels in the clinical study will not exceed baseline values.
Participants: 6 healthy adults of either sex, 21+ years old, who do not have gingivitis but
who have generalized gingival recession >1mm, 3 subjects must have at least 28 teeth.
Participants will be given a fluoride free toothpaste to use the day before the study and all
during the study. Participants will be reminded not to use fluoride toothpaste or other
fluoride products and to avoid fish and tea.
No toothbrushing or eating at all within an hour of any visit
Design: Observational study with each participant as his/her own control.
3 participants will 6 treated (Group A).3 participants will have 28 teeth treated each on the
facial aspect (Group B). Teeth with anterior fillings or decay at the gingival where staining
would show will not be treated.
Day 0 Procedures:
1. On day 0, the participant will be given 25 ml of de-ionized fluoride free water to swish
in the mouth and spit the entire contents into a 50 ml collection tube. This will be
done 3 times.
2. On day 0, 10 minutes after the rinsing and spitting, the participant will provide a
unstimulated salivary sample. The individual will be instructed to swallow once, and
allow saliva to pool in the mouth without swallowing, and then periodically spit the
saliva into a universal collection tube until 5 ml are collected. The tubes with saliva
will be stored on ice and then frozen at -20oC for transfer to the lab at the University
of Washington.
3. Day 0, Isolation and application of silver fluoride.
GROUP A (6 TEETH): 18 mcL will be expressed from a Hamilton syringe into a dappen dish,
and then a single preweighed microbrush will be used to apply the material to the tooth
surface after drying with cotton gauze. The 6 teeth will be treated consecutively until
all the material in the dappen dish will be used. Then the brush will be reweighed to
establish the non-applied amount.
GROUP B (28 TEETH) Measure out 3 mcL X number of teeth present into dappen dish.
Procedure is the same.
Application of silver fluoride. The quadrant will be isolated with cotton rolls, and
surrounding gingiva will be covered with petroleum jelly to provide additional
protection.
4. Day 0, after application, participant will be given 25 ml of fluoride free water to
rinse as in 1 above and water collected. This will be done 10 times.
DAY 1-6 Salivary Collection
5. Days 1-6, collection a single salivary sample at same time each day.
Procedure: Ten minutes before collection (on days 1-6), each individual will be given 100 ml
of de-ionized fluoride free water to rinse the mouth and swallow to increase hydration. The
individual will be instructed to swallow once, and allow saliva to pool in the mouth without
swallowing, and then periodically spit the saliva into a universal collection tube until 5 ml
are collected. The tubes with saliva will be stored on ice and then frozen at -20oC for
transfer to the lab at the University of Washington.
Measures: Fluoride will be measured using standard fluoride electrode analysis (Martinez-Mier
et al., 2011). Silver will be measured using Inductively Coupled Plasma-Mass Spectrometry
(EPA 6020a Rev.1 2007).
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04249336 -
Clinical Efficacy Of BioMin F, Colgate Sensitive Pro-Relief And Sensodyne Rapid Action Dentifrices In DH
|
Phase 3 | |
Completed |
NCT00763269 -
The Efficacy of a Toothpaste to Reduce Sensitivity
|
Phase 3 | |
Recruiting |
NCT06154941 -
Clinical Evaluation of Giomer Based Varnish Versus CPP-ACP Varnish in the Management of Dentin Hypersensitivity: a Randomized Clinical Trial
|
N/A | |
Completed |
NCT05501691 -
Effect of Diode Laser on Sensitive NCCLs Prior to Composite Restoration
|
N/A | |
Not yet recruiting |
NCT04484844 -
Clinical Evaluation of Efficacy of Shield Force Plus Varnish VS Sodium Fluoride on Dentin Hypersensitivity
|
Phase 2/Phase 3 | |
Completed |
NCT02936830 -
Effectiveness of Nanohydroxyapetite Paste on Reducing Dentin Hypersensitivity
|
Phase 4 | |
Completed |
NCT02931734 -
Assessment of Different Protocols for Cervical Dentin Hypersensitivity Treatment
|
N/A | |
Completed |
NCT04512625 -
Desensitizers in Reducing Post Tooth Preparation Sensitivity for a Fixed Dental Prosthesis
|
N/A | |
Completed |
NCT05623761 -
Toothpastes With Thermal Water for Oral Health
|
Phase 4 | |
Not yet recruiting |
NCT04731766 -
Effect of Using Different Varnishes on Dentin Hypersensitivity; Na Fluoride and Nano-silver Fluoride
|
N/A | |
Recruiting |
NCT05927831 -
Grape Seed Extract VS Low Level Laser Therapy for Dentin Hypersensitivity
|
N/A | |
Completed |
NCT03943095 -
Study to Characterize the Efficacy of a Dual Active Dentifrice for the Relief of Dentin Hypersensitivity
|
Phase 2 | |
Not yet recruiting |
NCT06276777 -
The Effect of Using Desensitizers Containing S-PRG In Treatment Of Dentin Hypersensitivity Over 6 Months: A Randomized Clinical Trial
|
N/A | |
Completed |
NCT04225247 -
Efficacy of Seventh Generation Bonding Agents as Short-Term Desensitizers Among Patients With Hypersensitivity
|
Phase 3 | |
Completed |
NCT04887181 -
The Effects of Different Dentin Hypersensitivity Treatment Methods on Quality of Life
|
N/A | |
Not yet recruiting |
NCT03061383 -
Reduction of Dentine Hypersensitivity Using 8% Arginine Based Toothpaste and 8% Strontium Acetate Based Toothpaste (DH)
|
N/A | |
Recruiting |
NCT03076944 -
Evaluation of Desensitization Protocols in Reduction of Dentin Hypersensitivity
|
N/A | |
Recruiting |
NCT06264453 -
A Study to Evaluate the Efficacy and Safety of KH001 in Patients With Dentin Hypersensitivity
|
Phase 2 | |
Recruiting |
NCT03083496 -
Clinical Evaluation of Different Potassium Oxalate Concentrations in Dentin Hypersensitivity Treatment
|
N/A | |
Completed |
NCT03965039 -
A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity
|
N/A |