Ignite Creation Date:
2024-05-06 @ 3:47 PM
Last Modification Date:
2024-10-26 @ 1:57 PM
Study NCT ID:
NCT04754763
Status:
COMPLETED
Last Update Posted:
2021-02-15
First Post:
2021-01-14
Brief Title:
A Comparative Study On The Effect Of Propolis And Dentine Bonding Agent In Treating Dentine Hypersensitivity
Sponsor:
Dow University of Health Sciences
Organization:
Dow University of Health Sciences
Study Overview
Official Title:
A Comparative Study On The Effect Of Propolis And Dentine Bonding Agent In Treating Dentine Hypersensitivity A Randomized Clinical Trial
Status:
COMPLETED
Status Verified Date:
2021-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Background
Dentine hypersensitivity DH causes considerable pain and discomfort to an individual due to number of stimuli on exposed dentine Different kinds of treatment strategies are used in the resolution of dentine hypersensitivity including the use of propolis and dentine bonding agent No study had compared the efficacy of propolis and dentine bonding agent
Objective
The objective of the study was to find out whether there is a difference in the efficacy of Propolis and seventh generation dentine bonding agent in reducing the dentine hypersensitivity Comparison within the groups and pairwise comparisons were also recorded in reducing dentine hypersensitivity
Methods
In this six month In- Vivo single blinded randomized clinical study a total number of 52 patients with complain of dentine hypersensitivity were selected in two groups after taking informed consent Group A and B received 30 ethanolic extract of propolis and dentine bonding agents respectively by a trained operator Recordings of dentine hypersensitivity were obtained at Day 0 before and after the application of experimental agents and also on Day 7 15 and 30 by the principal investigator Response was measured by Visual Analog Scale and Schiff Cold Air Sensitivity Scale Statistical Package for the Social Sciences SPSS version 20 was used to analyze the data with level of significance set at p 005 Friedman test was applied to see the comparison within groups and Wilcoxon Signed Rank test was used for Pairwise comparison Mann Whitney U-Test was applied for comparison between groups
Dentine hypersensitivity DH causes considerable pain and discomfort to an individual due to number of stimuli on exposed dentine Different kinds of treatment strategies are used in the resolution of dentine hypersensitivity including the use of propolis and dentine bonding agent No study had compared the efficacy of propolis and dentine bonding agent
Objective
The objective of the study was to find out whether there is a difference in the efficacy of Propolis and seventh generation dentine bonding agent in reducing the dentine hypersensitivity Comparison within the groups and pairwise comparisons were also recorded in reducing dentine hypersensitivity
Methods
In this six month In- Vivo single blinded randomized clinical study a total number of 52 patients with complain of dentine hypersensitivity were selected in two groups after taking informed consent Group A and B received 30 ethanolic extract of propolis and dentine bonding agents respectively by a trained operator Recordings of dentine hypersensitivity were obtained at Day 0 before and after the application of experimental agents and also on Day 7 15 and 30 by the principal investigator Response was measured by Visual Analog Scale and Schiff Cold Air Sensitivity Scale Statistical Package for the Social Sciences SPSS version 20 was used to analyze the data with level of significance set at p 005 Friedman test was applied to see the comparison within groups and Wilcoxon Signed Rank test was used for Pairwise comparison Mann Whitney U-Test was applied for comparison between groups
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None