Comparative Evaluation of Post-endodontic Pain Using Two Rotary Instrumentation Systems

NCT ID: NCT02621034

Last Updated: 2016-06-06

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-12-31

Study Completion Date

2016-03-31

Brief Summary

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In this study the investigators aim to compare the post-operative pain using two single-file endodontic rotary systems : Reciproc and One shape.

Detailed Description

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Comparison of the post operative pain with two rotary systems including Reciproc and One shape.

Confounding factors were neutralized and the rotary systems were compared.

Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Control

K-file hand instrumentation

Group Type EXPERIMENTAL

Control

Intervention Type PROCEDURE

K-file hand instrumentation

Reciproc

rotary reciprocating protocol

Group Type EXPERIMENTAL

Reciproc

Intervention Type PROCEDURE

reciprocating rotary instrument

One shape

one shape continuous rotation protocol

Group Type EXPERIMENTAL

One shape

Intervention Type PROCEDURE

full rotation protocol

Interventions

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Control

K-file hand instrumentation

Intervention Type PROCEDURE

Reciproc

reciprocating rotary instrument

Intervention Type PROCEDURE

One shape

full rotation protocol

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Systematically healthy patients
* First or second molars with irreversible pulpitis without periapical pathosis.
* Single visit endodontic treatment

Exclusion Criteria

* Root canal retreatment
* Pregnancy
* The presence of a difficult root canal anatomy
* Internal or external resorption
* Teeth with open apices
* Any accident of complication occurred during treatment
* Presence of periapical lesion, abscess or sinus tract
Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Zahedan University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Eshagh Ali Saberi, DDS,MS

Role: STUDY_DIRECTOR

Head of the department of Endodontics, Zahedan university of medical sciences

Locations

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Zahedan Dental School

Zahedan, , Iran

Site Status

Countries

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Iran

Other Identifiers

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SRH-1

Identifier Type: -

Identifier Source: org_study_id

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