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Comparison Between M-Pro and ProTaper Next

Symptomatic Irreversible Pulpitis Clinical Trial

Official title:
Comparison of Postoperative Pain After Root Canal Instrumentation Using M-Pro and ProTaper Next in Molars With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial

Clinical Trial Summary

Comparing the postoperative pain resulting after mechanical instrumentation using M-pro files versus that resulting after using ProTaper Next rotary files in lower molar with symptomatic Irreversible pulpitis molars.

Clinical Trial Description

Lower molars with symptomatic Irreversible pulpitis molars are selected according to the eligibility and exclusion criteria and patients are then randomized to receive treatment either using M-pro Files or ProTaper Next files. Postoperative pain is then assessed using the Numerical Rating scale 6, 12, 24, 48 and 72 hours post-operatively . After completing the treatment, patients will instructed to take placebo if they feel pain and will be asked to provide the quantity of placebo intake until 72 hrs. In case of pain not relieved by placebo, after recording the amount of pain, the patient will be instructed to take an alternative line of pain control (Ibuprofen 400mg tablets every 6 hours). The amount and frequency of Ibuprofen intake will be recorded. ;

Study Design

Related Conditions & MeSH terms

  • Pulpitis
  • Symptomatic Irreversible Pulpitis
Clinical Trial Details
NCT number NCT03692039
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date October 1, 2018
Completion date October 1, 2019
View Details
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