Incidence of Postoperative Pain After Glide Path Preparation Using Three Different Instruments
Postoperative Pain
About this trial
This is an interventional treatment trial for Postoperative Pain focused on measuring Glide path, postoperative pain, R-Pilot, ProGlider
Eligibility Criteria
Inclusion Criteria:
- Patients with no systemic disease or condition
- Patients having a maxillary or mandibular teeth diagnosed with one of the plural and periodontal diseases (asymptomatic irreversible pulpitis, symptomatic irreversible pulpitis, symptomatic apical periodontitis or asymptomatic apical periodontitis)
Exclusion Criteria:
- Patients, who were diagnosed with acute or chronic apical abscesses
- Patients showing signs of systemic infection
- Patients with allergies to local anesthetic agents,
- Patients who are taking medication (analgesic, antibiotic or anti-inflammatory drugs) during the 7 days before the procedure
- Patients presenting with multiple teeth requiring treatment or having a progressive periodontal disease
Sites / Locations
- Ondokuz Mayıs University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
R-Pilot®
ProGlider®
Manual preparation
R-Pilot® was operated by an endomotor (VDW Silver, Munich, Germany) at "Reciproc All" setting.
ProGlider® was operated by an endodontic motor (X-Smart, Dentsply Sirona, Ballaigues, Switzerland) with 16:1 contra angle at the suggested settings (300 rpm on display, 5 Ncm).
In the manual glide path group, glide path creation was performed with stainless steel #08, 10, 15 K-files used with "push and pull" motion. Instruments were used with a motion in which the instrument proceeds apically quarterly to the point of resistance, then is pulled out for debris removal. The procedure was repeated with each file until the working length was achieved and confirmed with an electronic apex locator (Root ZX Mini, Morita Corp., Kyoto, Japan).