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Assessment of Postoperative Pain Using Reciproc Versus One Shape Files in Patients With Irreversible Pulpitis

NCT02953912 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2016-11-03

No results posted yet for this study

Summary

To show whether One Shape rotary system differs from Reciproc reciprocating system in postoperative pain in patients with symptomatic irreversible pulpitis.

Conditions

  • Pulpitis - Irreversible

Interventions

PROCEDURE

Reciproc single-file

The Reciproc is a single-file nickel-titanium systems , made of a special nickel-titanium (NiTi) alloy called M-Wire created by innovated thermal treatment process which increases flexibility and improved resistance to cyclic fatigue

PROCEDURE

One Shape single-file

One Shape is one of the few single file made of austenite 55- NiTi alloy characterized by different cross sectional designs ,it is used in continuous clockwise rotation for a quick and safe root canal preparation due to its flexibility and minimal fatigue.In addition to , the electropolished safety tip instrument for enhanced cutting efficiency and it is delivered in a sterile blister for single use.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Shaimaa I Gawdat, Lecturer · Department of endodontics - Faculty of Oral and Dental medicine - CU

  • Angie G Ghoneim, Professor · Department of endodontics - Faculty of Oral and Dental medicine - CU

  • Asmaa M kamel, Student · Department of endodontics - Faculty of Oral and Dental medicine - CU

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
2017-10-31
Completion
2018-01-31

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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 NCT02953912 on ClinicalTrials.gov