Clinical Trial

Effect of Integrated Apex Locator Motor Modes on Postoperative Pain in Endodontic Retreatment

Study acronym: EAL-Pain
Completed
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Summary
This randomized controlled clinical trial aimed to evaluate the effect of different integrated electronic apex locator (EAL) modes on postoperative pain following nonsurgical endodontic retreatment. A total of 144 patients requiring retreatment of mandibular premolar teeth with periapical lesions were randomly assigned to four groups. In the control group, working length was determined using a conventional electronic apex locator. In the experimental groups, an integrated EAL motor was used with three different modes: apical reverse, apical slow down, and apical stop. All procedures were performed under standardized conditions. Postoperative pain was assessed using a numeric rating scale (NRS) at 6 and 12 hours and on days 1, 2, 3, 5, and 7 after treatment. The study aimed to determine whether simultaneous working length control using integrated EAL modes influences postoperative pain compared with conventional working length determination.
Trial Details
NCT Number NCT07527897
Lead Sponsor Recep Tayyip Erdogan University
Conditions Apical Periodontitis, Postoperative Pain, Endodontic Retreatment
Enrollment 144 participants
Start Date 2025-08-13
Primary Completion 2025-10-10 (estimated)
Study Completion 2025-10-17 (estimated)
Updated on ClinicalTrials.gov 2026-04-14