Pain Intensity After Root Canal Instrumentation

Pain, Postoperative Clinical Trial

Official title:

Assessment of Pain Intensity After Instrumentation by MPRo and Hyflex Rotatry Files in Molars With Irreversible Pulpitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04216940
• Other study ID #: pain intensity
• Status: Completed
• Phase: N/A
• Start date: February 10, 2019
• Est. completion date: August 28, 2019

Study information

• Verified date: January 2020
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Assess the pain intensity in a two visit treatment of molars with irreversible pulpitis after instrumentation with two rotary systems Mpro and Hyflex files.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: August 28, 2019
• Est. primary completion date: August 28, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 25 Years to 40 Years

Eligibility

Inclusion Criteria:

• mandibular molars with acute pulpitis

Exclusion Criteria:

• badly decayed non-restorable molars

• medically compromised patients

Related Conditions & MeSH terms

• Pain
• Pain, Postoperative

Intervention

Device:
• mechanical preparation of root canal system
Assess the pain intensity in a two-visit treatment of molars with irreversible pulpitis after instrumentation with two different rotary Nickle Titanium systems

Locations

Country	Name	City	State
Egypt	Ain Shams University	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain felt after mechanical instrumentation in the first visit	using Numeric Rating Scale (NRS) the participant will be asked to verbally rate their pain on a scale from 0 to 10, with 0 equal to no pain and 10 equal to worst possible pain	up to 72 hours