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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.
Full 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
Enrollment
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Inclusion criteria
• Medically free patients.
Exclusion criteria
• Teeth with unfavorable conditions for rubber-dam application.
Primary purpose
Allocation
Interventional model
Masking
30 participants in 3 patient groups
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Central trial contact
Reham Hassan, Assoc Prof; Mohamed Salah Hegazi
Data sourced from clinicaltrials.gov
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