Ignite Creation Date:
2024-05-06 @ 7:57 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06197555
Status:
COMPLETED
Last Update Posted:
2024-01-09
First Post:
2023-12-12
Brief Title:
Comparision of the Clinical Efficacy of Different Desensitizing Toothpastes
Sponsor:
Altinbas University
Organization:
Altinbas University
Study Overview
Official Title:
Comparision of the Clinical Efficacy of Different Desensitizing Toothpastes
Status:
COMPLETED
Status Verified Date:
2023-12
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:
Dentin hypersensitivity is a common problem in society Untreated hypersensitivity affects the patients quality of life complicates plaque control and increases the risk of caries and periodontal disease This study aimed to evaluate the clinical efficacy of desensitizing toothpastes containing sodium fluoride stannous fluoride nano-hydroxyapatite 8 arginine and calcium carbonate
Fourty eight patients with at least two teeth with positive responses to air and mechanical stimulus were included in the study and were divided into four groups Sodium fluoride Colgate Cavity Protection in group A stannous fluoride Oral B Gum Calm Sensitivity in group B nano-hydroxyapatite ApaCare in group C and 8 arginine and calcium carbonate combination in group D Colgate Sensitive Pro- ReliefTM were used by the patients continuously for 16 weeks Dentin hypersensitivity by using VAS and Shiff scores and periodontal parameters were evaluated at baseline 2nd week 4th week and last 16th week
Fourty eight patients with at least two teeth with positive responses to air and mechanical stimulus were included in the study and were divided into four groups Sodium fluoride Colgate Cavity Protection in group A stannous fluoride Oral B Gum Calm Sensitivity in group B nano-hydroxyapatite ApaCare in group C and 8 arginine and calcium carbonate combination in group D Colgate Sensitive Pro- ReliefTM were used by the patients continuously for 16 weeks Dentin hypersensitivity by using VAS and Shiff scores and periodontal parameters were evaluated at baseline 2nd week 4th week and last 16th week
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?:
False
Is an FDA AA801 Violation?:
None