Pain, Postoperative Pain Pathologic Processes Postoperative Complications Signs and Symptoms Clinical Trial
Official title:
Comparative Evaluation of Post Endodontic Pain Following Root Canal Treatment With Two Rotary System: Neolix & Waveone
NCT number | NCT02768311 |
Other study ID # | 7354 |
Secondary ID | |
Status | Active, not recruiting |
Phase | N/A |
First received | May 9, 2016 |
Last updated | May 10, 2016 |
Start date | May 2016 |
Verified date | April 2016 |
Source | Zahedan University of Medical Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | Iran: Ethics Committee |
Study type | Interventional |
Today, dentists tend to use rotary systems. Despite the increasing diversity of these systems as well as a few studies on the prevalence of pain after root canal treatment by rotary systems, And in particular, comparing the amount of pain after treatment, between systems RECIPROCAL AND FULL ROTATION single-file, the aim of this study was to evaluate the effect of applying canal preparation by the system, Neolix and WaveOne, on the prevalence of pain after endodontic treatments.
Status | Active, not recruiting |
Enrollment | 150 |
Est. completion date | |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 20 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Age range 20-50 years, - the systemically healthy, - first or second molar teeth require root canal therapy, - irreversible Pulpitis signed without the apical, - root canal curvature of less than 25 degrees, according to Schneider techniques. Exclusion Criteria: - Root canal treatment, - history of medication (antibiotics, NSAID, opiates) of the patient 12 hours before treatment, - pregnancy, - complex anatomy, - channels blocked in the x-ray plate, - internal and external resorption, - open apex teeth, - periodontal disease, - inflammation and abscesses, - sinus tract, - presence of radiographic lesions, - tooth sensitivity to percussion, - absence of occlusal contact. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
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Zahedan University of Medical Sciences |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Information regarding post-operation pain is gathered via a patient using questionnaire and is measured via the visual analogue scale | 12 month | Yes |