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Clinical Trials/NCT03412318
NCT03412318
Completed
Not Applicable

Evaluation of the Effect of Root Canal Preparation by TF and M-Pro on Post-Operative Pain After Single Visit Endodontic Treatment: A Blinded Randomized Clinical Trial Therapeutic Study.

Cairo University1 site in 1 country48 target enrollmentOctober 6, 2018
ConditionsAcute Pulpitis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Pulpitis
Sponsor
Cairo University
Enrollment
48
Locations
1
Primary Endpoint
Post-operative pain
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

A study to comparatively evaluate the post operative pain between root canal preparation by reciprocating file (TF) and full rotation file (M-Pro) in patients with single rooted teeth with acute irreversible pulpits.

Detailed Description

Teeth with symptomatic irreversible pulpitis are selected according to the eligibility and exclusion criteria and patients are then randomized to receive treatment after using Twisted files or M-pro files. The treatment is done in single visit. The postoperative pain is then assessed using the Numerical Rating Scale 6,12, 24 and 48 hours post-instrumentation.

Registry
clinicaltrials.gov
Start Date
October 6, 2018
End Date
January 22, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmad Abdul Aziz Almorad

Principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients in good health (American Society of Anesthesiologists Class II or higher).
  • Patients having symptomatic irreversible pulpitis in their single rooted teeth.
  • Age range is between 20 and 60 years.
  • Patients who can understand numerical rating scale (NRS).
  • Patients able to sign informed consent.

Exclusion Criteria

  • Patients with positive percussion test.
  • Patients having history of necrosis with or without apical pathosis.
  • Patients have sinus tract or fistula extra oral or intraoral.
  • Pregnant or mentally retarded patients.
  • Teeth with grade 2 or 3 mobility.

Outcomes

Primary Outcomes

Post-operative pain

Time Frame: 2 days

Post-operative pain assessed after treatment using the NRS pain scale

Study Sites (1)

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