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Assessment of Postoperative Pain After Using Reciproc Versus One Shape NiTi Systems

NCT02940704 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2018-07-26

No results posted yet for this study

Summary

* The aim of this study is to assess the postoperative pain and the intake of analgesic medication after using Reciproc single-file reciprocating system or One Shape single-file continuous rotary system in patients with symptomatic irreversible pulpitis.
* Patients will be diagnosed to determine whether they are eligible for the inclusion criteria of this study or not. Patients who are eligible will then start their root canal treatment on the same visit and to be completed in one visit only. Patients will be phone called in order to record the intensity of pain, amount and frequency of analgesic intake at 6, 12, 24, 48 and 72 hours after treatment.

Conditions

  • Pulpitis

Interventions

PROCEDURE

Reciproc

* Canals will be instrumented using Reciproc reciprocating system set on an electric motor, with adjusted torque and speed according to the manufacturer's instructions. * There is no need for coronal preflaring with a Gates Glidden drill or an orifice opener since the design of the Reciproc instrument allows any obstructions in the coronal third to be removed, as claimed by the manufacturer. * Reciproc file selection: R40 (40/0.06) is to be used.

PROCEDURE

One Shape

* Coronal preflaring will be performed using Gates Glidden drill. * Canals will be instrumented using One Shape single-file (25/0.06) set on an electric motor with adjusted torque and speed according to the manufacturer's instructions. * For wide canals, One Shape Apical (30/0.06, 37/0.06) will be used.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Michel K Elias, Resident · Faculty of Oral and Dental Medicine - Cairo University

  • Hebatallah M El-Far, Professor · Faculty of Oral and Dental Medicine - Cairo University

  • Shaimaa I Gawdat, Lecturer · Faculty of Oral and Dental Medicine - Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2017-05-31
Completion
2018-01-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02940704 on ClinicalTrials.gov