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The Success Rate of Cryotherapy Application in Primary Molars With Signs of Irreversible Pulpitis

Pain, Procedural Clinical Trial

Official title:
The Success Rate of Cryotherapy Application in Primary Molars With Signs of Irreversible

Clinical Trial Summary

The study is designed as a randomized controlled trial with two parallel groups. Children aged 5-9 years with primary molars from suffered symptomatic signs of irreversible pulpitis will be randomly assigned into two groups. The first group (experimental group) will be injected with 4% articaine 1:100.000 epinephrine (inferior alveolar nerve block). For the second group, the mandibular second primary molars will be anesthetized using 4% articaine 1:100.000 epinephrine using inferior alveolar nerve block.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05267847
Study type Interventional
Source Minia University
Contact
Status Recruiting
Phase N/A
Start date February 22, 2022
Completion date April 30, 2022
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