Post-operative Pain Reduction

Effects of the Elements Clinical Trial

Official title:
Post-operative Pain Reduction After Application of Three Intracanal Medicament Within Necrotic Root Canals and Pulp

Status Recruiting

Clinical Trial Summary

Recruited patients with necrotic pulp after application of conventional calcium hydroxide paste are assigned to group, Calcium hydroxide nanoparticle group and Combined Calcium hydroxide with silver nanoparticle group and record postoperative pain afterwards.

Clinical Trial Description

The investigator will recruit patients who are found eligible to the criteria, conventional calcium hydroxide paste , Calcium hydroxide nanoparticle and Combined Calcium hydroxide with silver nanoparticle . After 48 hours, patients will be randomly assigned to removal of intracanal medication

After the visit, patients will be asked to record post operative pain by Numerical Rating Scale)in a given sheet ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04338633
Study type	Interventional
Source	Minia University
Contact	Mohamed Salah Hegazi
Phone	+201224014179
Email	mshegazi2006@gmail.com
Status	Recruiting
Phase	N/A
Start date	April 2020
Completion date	November 2020

View Details

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