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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02621034
Other study ID # SRH-1
Secondary ID
Status Completed
Phase N/A
First received November 29, 2015
Last updated March 11, 2016
Start date June 2015
Est. completion date March 2016

Study information

Verified date July 2015
Source Zahedan University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date March 2016
Est. primary completion date February 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 50 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
k file
hand instrumentation
Reciproc
reciprocating rotary instrument
One shape
full rotation protocol

Locations

Country Name City State
Iran, Islamic Republic of Zahedan Dental School Zahedan

Sponsors (1)

Lead Sponsor Collaborator
Zahedan University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Information regarding post-operation pain is gathered from the patients using questionnaires and is measured via the visual analogue scale 6 months Yes
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