Evaluation of Postoperative Pain in Children
Postoperative Pain
About this trial
This is an interventional screening trial for Postoperative Pain focused on measuring postoperative pain, root canal treatment, reciprocal motion, rotary motion
Eligibility Criteria
Inclusion Criteria:
- Patients with first permanent mandibular molar teeth which had been diagnosed with symptomatic irreversible pulpitis with no periapical pathology or abscess were included in the study.
Exclusion Criteria:
- Patients who were on antibiotics or analgesics preoperatively were not included in the study.
Sites / Locations
- Ege University
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Protaper Next
Reciproc Blue
Protaper Next group (n=25): The instrumentation of mesial and distal canals were done according to manufacturer's recommendations using X1 and X2 (25.06) at a rotational speed of 300 rpm. Then X3 and X4 (40.06) instruments were used to enlarge distal canals in order to compare the results with the Reciproc Blue group. The root canals were irrigated with 2 ml of %2,5 sodium hypochlorite after each instrument exchange.
Reciproc Blue group (n=25) : The canals were shaped with in accordance with the manufacturer's recommendations. R25 (25.08) instrument was introduced into the canal with slow pecking movement within a 3 mm range each time. The flutes and remnants were cleaned after 3 pecking moves. Then R40 instrument (40.06) was selected to shape the distal canals as the #20 K file was passively introduced to the working length. The root canals were irrigated with 2 ml of %2,5 sodium hypochlorite after each instrument exchange.