Ignite Creation Date:
2024-05-06 @ 2:36 PM
Last Modification Date:
2024-10-26 @ 1:33 PM
Study NCT ID:
NCT04365270
Status:
COMPLETED
Last Update Posted:
2021-01-12
First Post:
2019-12-06
Brief Title:
Antibacterial Effect and Clinical Performance of Chitosan Modified Glass Ionomer
Sponsor:
Ain Shams University
Organization:
Ain Shams University
Study Overview
Official Title:
The Antimicrobial Activity and Clinical Performance of Chitosan-modified Glass Ionomer A Randomized Clinical Trial
Status:
COMPLETED
Status Verified Date:
2021-01
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 is a randomized clinical trial that assesses the clinical success and the antibacterial effect on carious dentine of glass ionomer when modified with Chitosan andor Titanium dioxide nano particles vs the control group of modification with Chlorhexidine as control when used in primary molars
Detailed Description:
Participants will be recruited from the acquitted to the clinic of pediatric dentistry department Faculty of Dentistry of Ain Shams University random allocation of the participants where indirect pulp capping is indicated so that modified Glass ionomer would be used as the filling material
partial removal of caries is done then caries sample would be taken and sent for a microbiological evaluation and then cavity dimensions is recoded finally placement of the modified glass ionomer in the prepared cavity
In a total period of 9 months the patients will be followed every 3 months for clinical evaluation and in the final visit the filling would be removed and another bacterial sample would be taken for comparison then a permanent filling is placed
partial removal of caries is done then caries sample would be taken and sent for a microbiological evaluation and then cavity dimensions is recoded finally placement of the modified glass ionomer in the prepared cavity
In a total period of 9 months the patients will be followed every 3 months for clinical evaluation and in the final visit the filling would be removed and another bacterial sample would be taken for comparison then a permanent filling is placed
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