Irrigation Activation
Conditions
Brief summary
Irrigation activation in endodontics is considered now a very important step for the success of root canal treatment. In this study, the investigator will examine the effect of two recent activation systems ( XP-endo Finisher file and the new sonic EDDY system) in comparison with the conventional needle irrigation on irrigant penetration depth into root canals using radiopaque contrast media and digital radiography and on the postoperative pain after single-visit endodontic treatment using a visual analog scale.
Interventions
irrigation activation using 3 different irrigation activation systems including xp endo finisher file , new sonic eddy system and conventional needle syringe irrigation
Sponsors
Study design
Intervention model description
the study will evaluate 3 groups of patients each consists of 10 participants receiving different type of irrigation activation.
Eligibility
Inclusion criteria
* Asymptomatic vital/non vital teeth requiring root canal treatment. * Teeth with sound periodontal apparatus. * Teeth without pus or inflammatory exudates draining through the canal. * Teeth without anatomic variations. * Teeth with sinus tract. * Teeth without history of trauma. * Patients not on analgesics or sedative medication prior to root canal therapy
Exclusion criteria
* • Patients with any systemic diseases. * Pregnant or lactating patients. * Immunocompromised patients. * Apparently thin roots in which apical preparation with #40 file would be overzealous. * Patient allergic to anything used in this procedure especially rubber dam material and Iohexol (radiographic contrast media). * Teeth with calcified canals. * Patients with acute apical periodontitis, acute apical abscess, and weeping canals. * Necrotic painful teeth with the absence of sinus tract for drainage.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| irrigant penetration depth | through study completion, an average of 3 months | measurement of irrigant penetration depth using radioaque media and digital radiography |
| postoperative pain | through study completion, an average of 3 months | evaluation of postoperative pain using visual analog scale VAS with scores from 0 to 100. score 0 indicated no pain while score 100 indicates maximum pain |
Countries
Egypt