Clinical Trials Directory

Trials / Completed

CompletedNCT03692039

Comparison Between M-Pro and ProTaper Next

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREM-pro files in rotating motionAn endodontic file that has controlled memory properties
PROCEDUREProTaper Next files in rotating motionAn endodontic file that has an off center mass of rotation

Timeline

Start date
2018-10-01
Primary completion
2019-10-01
Completion
2019-10-01
First posted
2018-10-02
Last updated
2020-07-14

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03692039. Inclusion in this directory is not an endorsement.