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Clinical Trial Summary

This study investigates the effect of the addition of titanium dioxide nanoparticles to denture base materials on their retention compared to that of the unmodified denture base materials.


Clinical Trial Description

All patients will be randomly allocated to two equal groups either with the protocol I or II (5 in each group) with an allocation ratio of 1:1 through a computer-generated sequence by a spreadsheet (Excel, Microsoft Office 2010; Microsoft Corp). The group with the protocol I will use the modified dentures with titanium dioxide nanoparticles (TiO2NP) during the first month, followed by no use of the first denture and the use of their old relined dentures instead for 1 month (washout), and then the use of the unmodified dentures for 1 month; the group with the protocol II will use the unmodified dentures during the first month, followed by no use of the first denture and the use of their old relined dentures instead for 1 month (washout), and then the use of the modified dentures TiO2NP for 1 month. Assessment of retention will be done immediately and 1 month after denture insertion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04991064
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date February 12, 2017
Completion date June 15, 2017

See also
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Completed NCT03037307 - A Clinical Bite Force Study of Two Marketed Adhesives Against no Adhesive N/A