Ignite Creation Date:
2024-07-17 @ 11:33 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06485024
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-06-26
Brief Title:
Effect of Modeling Resin on Anterior Direct Composite Veneer
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Clinical Performance of Direct NanoHybrid Resin Composite Veneer Restorations Applied With or Without Modeling Resina Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
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:
the study will be conducted to evaluate the clinical performance of direct Nanohybrid resin composite veneer restorations applied with or without modeling resin
Detailed Description:
ChatGPT This study aims to investigate the impact of modeling resin on the clinical performance of direct nanohybrid resin composite veneer restorations in anterior teeth Resin composites are widely used in dental restorations due to their aesthetic qualities but issues like discoloration and surface roughness can affect their longevity and patient satisfaction Modeling resin used to aid in composite placement and sculpting has become common but concerns exist regarding its effects on composite properties particularly long-term color stability
The research will employ a randomized controlled trial design with a two-arm parallel approach Adult patients 18-45 years with anterior tooth defects suitable for composite veneer restoration will be recruited The intervention group will receive nanohybrid resin composite with modeling resin while the comparator group will receive the composite without modeling resin Outcomes will be assessed using modified USPHS criteria including color stability color match anatomical form marginal adaptation marginal discoloration retention rate presence of secondary caries and postoperative sensitivity at baseline and at follow-up intervals of 1 3 6 and 12 months
Statistical analysis will involve independent t-tests for intergroup comparisons and repeated measures ANOVA for intragroup comparisons with a significance level set at 005 The study aims to determine if the use of modeling resin influences the clinical outcomes of resin composite veneer restorations Ethics approval will be obtained and confidentiality of participant data will be strictly maintained throughout the study period
Overall this research seeks to provide insights into optimizing the application of resin composites in dental practice to enhance patient outcomes and satisfaction
The research will employ a randomized controlled trial design with a two-arm parallel approach Adult patients 18-45 years with anterior tooth defects suitable for composite veneer restoration will be recruited The intervention group will receive nanohybrid resin composite with modeling resin while the comparator group will receive the composite without modeling resin Outcomes will be assessed using modified USPHS criteria including color stability color match anatomical form marginal adaptation marginal discoloration retention rate presence of secondary caries and postoperative sensitivity at baseline and at follow-up intervals of 1 3 6 and 12 months
Statistical analysis will involve independent t-tests for intergroup comparisons and repeated measures ANOVA for intragroup comparisons with a significance level set at 005 The study aims to determine if the use of modeling resin influences the clinical outcomes of resin composite veneer restorations Ethics approval will be obtained and confidentiality of participant data will be strictly maintained throughout the study period
Overall this research seeks to provide insights into optimizing the application of resin composites in dental practice to enhance patient outcomes and satisfaction
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