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3D Instrumentation Versus Rotary Instrumentation

NCT03285334 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-09-18

No results posted yet for this study

Summary

enrollment of the patient after diagnosis, radiographic evaluation, and signing the informed consent.

allocation of the patient to either intervention or control group. After anaesthesia and access cavity, the first root canal sample will be taken. Endodontic treatment will be completed in one visit. The second root canal sample will be taken. Patients will be asked to evaluate their postoperative pain level using VAS scale at 6, 12, 24 hours, and daily up to 5 days. Patients will record the number of analgesics if any taken.

Conditions

  • Postoperative Pain

Interventions

DEVICE

XP-endo Shaper

mechanical preparation in a 3D manner using Xp-endo Shaper

DEVICE

iRace files

rotary mechanical preparation

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Radwa Emara · faculty of oral and dental medicine - cairo university

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-11-30
Primary Completion
2018-02-28
Completion
2018-11-30

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 NCT03285334 on ClinicalTrials.gov