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Clinical Trial Summary

There is a lack of long-term clinical studies comparing different restorative materials; most of the available studies have only looked at class I cavities or examined post-operative sensitivity in non-caries cervical lesions. The purpose of this study is to measure postoperative sensitivity in clinical settings at 3-month intervals for class 1 and 2 direct posterior restoration


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05882760
Study type Interventional
Source Liaquat University of Medical & Health Sciences
Contact Priya Rani, BDS
Phone 03365179755
Email priya.harjani@hotmail.com
Status Recruiting
Phase Phase 4
Start date June 1, 2023
Completion date December 31, 2024

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