Ignite Creation Date:
2025-12-24 @ 9:59 PM
Ignite Modification Date:
2025-12-24 @ 9:59 PM
Study NCT ID:
NCT04509232
Status:
COMPLETED
Last Update Posted:
2021-09-27
First Post:
2020-08-08
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Assessing Parental Acceptance to Silver Diamine Fluoride Staining Before and After Masking the Colour With Glass Ionomer
Sponsor:
Dina Bassam Mohamed Ahmed
Organization:
Study Overview
Official Title:
"Parental Perception and Acceptance of the Utilization of Silver Diamine Fluoride on Their Child's Anterior and Posterior Teeth Before and After Masking the Colour With Glass Ionomer"
Status:
COMPLETED
Status Verified Date:
2021-09
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:
Assessing Parents acceptance for the colour of Silver Diamine Fluoride on their Children anterior and posterior teeth before and after masking its colour with Glass Ionomer.
Detailed Description:
Sample size estimation Sample size estimation was based on the primary outcome of interest The final sample size was 41 children per group (total sample size = 82 children)
Patients will be recruited randomly from outpatient clinic of the Department of Pediatric Dentistry and Dental Public Health, Faculty of Dentistry, Ain Shams University. A signed informed consent to the parents' and also an insent to child,outlined by the Ethical Committee, Faculty of Dentistry, Ain Shams University will be obtained before the conduction of the study.
All examination procedures will be done by the same operator to ensure standardization.
Moreover, all patients will receive oral health education in regard to dietary and oral hygiene habits.
Excluded carious primary molars will be scheduled to receive the appropriate treatment.
Before applying any procedures medical history for any silver products allergy (SDF allergy) will be assessed by asking the child's parent.
Materials:
38%SDF
Conditioner 3M ESPE
High strength hand mix chemical cure glass ionomer
Patient withdrawal
Patient who don't comply to the oral hygiene given will be excluded from the study.
Patients who are not willing to continue in the study will have the right to quit at any time without loss of any benefits.
Data Management
Patient information will be gathered and stored in the patient examination chart of the outpatient clinic, Department of Pediatric Dentistry, faculty of Dentistry, Ain Shams University.
All information will be kept as a hard copy and as an electronic one as well. Patient information will be guarded as confidential information that should never be revealed at all times.
Adverse Event Reporting
SDF is not expected to have any adverse effects on healthy subjects, yet failure of treatment, recurrent caries, abcess formation or pulpal affection may be an issue of concern, that will be avoided by the continuous follow up sessions.
Statistical Analysis
Sample size estimation was based on the primary outcome of interest, which is to test whether there's a significant difference in parent satisfaction between the parents of children receiving SDF and those receiving SDF followed by ART restorations. The predicted sample size for comparing parent satisfaction score was found to be 34 children per group (total sample size = 68 children), by assuming an α level of 0.05 and β level of 0.2 (power = 80%). The effect size d was calculated based on the findings of M. Jiang, et al., and the allocation ratio was set at 1. After adjusting for 20% dropout, the final sample size was 41 children per group (total sample size = 82 children). Sample size calculation was performed using G\*Power software version 3.1.4 for MS Windows.
Patients will be recruited randomly from outpatient clinic of the Department of Pediatric Dentistry and Dental Public Health, Faculty of Dentistry, Ain Shams University. A signed informed consent to the parents' and also an insent to child,outlined by the Ethical Committee, Faculty of Dentistry, Ain Shams University will be obtained before the conduction of the study.
All examination procedures will be done by the same operator to ensure standardization.
Moreover, all patients will receive oral health education in regard to dietary and oral hygiene habits.
Excluded carious primary molars will be scheduled to receive the appropriate treatment.
Before applying any procedures medical history for any silver products allergy (SDF allergy) will be assessed by asking the child's parent.
Materials:
38%SDF
Conditioner 3M ESPE
High strength hand mix chemical cure glass ionomer
Patient withdrawal
Patient who don't comply to the oral hygiene given will be excluded from the study.
Patients who are not willing to continue in the study will have the right to quit at any time without loss of any benefits.
Data Management
Patient information will be gathered and stored in the patient examination chart of the outpatient clinic, Department of Pediatric Dentistry, faculty of Dentistry, Ain Shams University.
All information will be kept as a hard copy and as an electronic one as well. Patient information will be guarded as confidential information that should never be revealed at all times.
Adverse Event Reporting
SDF is not expected to have any adverse effects on healthy subjects, yet failure of treatment, recurrent caries, abcess formation or pulpal affection may be an issue of concern, that will be avoided by the continuous follow up sessions.
Statistical Analysis
Sample size estimation was based on the primary outcome of interest, which is to test whether there's a significant difference in parent satisfaction between the parents of children receiving SDF and those receiving SDF followed by ART restorations. The predicted sample size for comparing parent satisfaction score was found to be 34 children per group (total sample size = 68 children), by assuming an α level of 0.05 and β level of 0.2 (power = 80%). The effect size d was calculated based on the findings of M. Jiang, et al., and the allocation ratio was set at 1. After adjusting for 20% dropout, the final sample size was 41 children per group (total sample size = 82 children). Sample size calculation was performed using G\*Power software version 3.1.4 for MS Windows.
Study Oversight
Has Oversight DMC:
False
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?: