Clinical Trial to Compare the Efficacy of a Fluoride Gel and a Dental Bonding Agent in Treatment of Tooth Sensitivity
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02919202|
Recruitment Status : Completed
First Posted : September 29, 2016
Last Update Posted : May 5, 2017
|Condition or disease||Intervention/treatment||Phase|
|Dentin Sensitivity||Procedure: Colgate Fluoride Varnish Suspension. 2.26% Sodium Fluoride. Procedure: Self-etching Dentine Bonding Agent||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||26 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Official Title:||A Randomised Controlled Trial Investigating a Comparison of Fluoride Varnish vs Self-Etching Dentine Bonding Agent in the Reduction of Cervical Dentine Sensitivity in Patients Attending a General Dental Practice in West Sussex, UK.|
|Actual Study Start Date :||October 26, 2016|
|Actual Primary Completion Date :||January 4, 2017|
|Actual Study Completion Date :||January 4, 2017|
Experimental: Fluoride Varnish
Colgate Fluoride Varnish Suspension. 2.26% Sodium Fluoride.
Procedure: Colgate Fluoride Varnish Suspension. 2.26% Sodium Fluoride.
Topical application to exposed dentine on one occasion.
Other Name: Duraphat Varnish
Active Comparator: SEDBA
Self-etching Dentine Bonding Agent. Scotchbond Universal by 3M ESPE. Topical application followed by light curing for 20 seconds.
Procedure: Self-etching Dentine Bonding Agent
Topical application to exposed dentine on one occasion followed by light-curing procedure.
Other Name: Scotchbond Universal
- Visual Analogue Scale [ Time Frame: 14 days ]to measure pain/sensitivity perception
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02919202
|Carfax Dental Practice|
|Horsham, West Sussex, United Kingdom, RH12 1EB|
|Principal Investigator:||Claire Parkin, PhD||University of Kent|