Evaluation the Post Operative Pain of Endodontic Treated Molar Tooth With Race and Reciprocal Systems Among Bandarabbas Patients in 2017

Endodontically Treated Teeth Clinical Trial

Official title:

Evaluation the Post Operative Pain of Endodontic Treated Molar Tooth With Race and Reciprocal Systems Among Bandarabbas Patients in 2017: A Double Blind Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03488836
• Other study ID #: 911150105
• Status: Recruiting
• Phase: Phase 2/Phase 3
• First received: February 4, 2018
• Last updated: April 4, 2018
• Start date: May 2, 2018
• Est. completion date: November 2, 2018

Study information

• Verified date: April 2018
• Source: Hormozgan University of Medical Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

extrusion of infected dentin into the periapical tissue has been suggested as a major source of pain after endodontic treatment. Although debris extrusion is an inevitable finding even when instrumentation is limited to the confines of the canal, different armamentarium seem to be associated with different amounts of debris extrusion. Studies on the effect of various rotary files on post-endodontic pain are very few and have yielded conflicting results with some favoring full-sequence and others leaning towards reciprocal rotary systems. This study aims at assessing the intensity of post-endodontic pain following two different rotary systems, Reciproc and race.

Methods: in this single-blind, parallel-grouped randomized clinical trial a total of 150 otherwise healthy patients aged between 20 to 50 years old with a pulpal status of irreversible pulpitis for one tooth in the upper or lower molar region were analyzed. A clinician performed the endodontic treatment in two groups, a group instrumented using race and a third group with instrumentation performed using Reciproc rotary systems.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 132
• Est. completion date: November 2, 2018
• Est. primary completion date: July 2, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

• Inclusion criteria: the otherwise healthy patients were aged between 20 to 50 years old with a pulpal status of irreversible pulpitis for one tooth in the upper or lower molar region.

Exclusion Criteria:

• Exclusion criteria: previous endodontic treatment; a history of drug intake including corticosteroids; opioids and NSAIDs in the previous 12 hours; pregnancy; complicated anatomy (curves greater than 25 degrees); calcifications; internal & external resorption; open apices; periodontal disease; swelling & abscess; presence of periapical lesions; sensitivity to percussion and lack of occlusal contact.

Related Conditions & MeSH terms

• Endodontically Treated Teeth
• Pain, Postoperative
• Tooth, Nonvital

Intervention

Procedure:
• reciproc
rotary reciprocating protocol
• race rotary
race rotary group protocol

Locations

Country	Name	City	State
Iran, Islamic Republic of	Dental clinic of BandarAbbas faculty of dentistry	Bandar Abbas	Hormozgan

Sponsors (1)

Lead Sponsor	Collaborator
Sajad Ansari Fard

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	change of the Visual analogue scale	change of the vas evaluation	6-12-18-24-48-72 hours