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Clinical Trial Summary

conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers


Clinical Trial Description

STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS. TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS, GROUP1: ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS. GROUP2: ALL CANALS WILL BE OBTURATED USING HIGH FLOW BIOCERAMIC SEALERS THAT ACCEPT WARM VERTICAL COMPACTION POST OPERATIVE PAIN IN THE TWO GROUPS WILL BE EVALUATED USING THE VISUAL ANALOUG SCALE AND COMPARED AT DIFFERENT TIME PERIODS (12H, 24H, 48H, 72H) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05729893
Study type Interventional
Source British University In Egypt
Contact sara tarek mohamed, bachelor
Phone 01007434392
Email sara.alsayed@bue.edu.eg
Status Recruiting
Phase N/A
Start date February 1, 2023
Completion date September 1, 2023

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