Clinical Trial

Selective Curettage and Tissue Adhesive in Endodontic Microsurgery

Study acronym: Microsurgery
Active, Not Recruiting
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Record status
This record was last updated January 20, 2026 (before its estimated January 29, 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of this randomized clinical trial is to determine whether selective curettage combined with cyanoacrylate tissue adhesive improves clinical outcomes in endodontic microsurgery compared with the conventional approach. The study purpose is to evaluate the postoperative healing associated with this conservative surgical protocol. The main questions it aims to answer are: Does selective curettage with tissue adhesive reduce postoperative pain, swelling, and complications compared to complete curettage with suturing? How does selective curettage affect clinical and radiographic healing of persistent periapical lesions? Researchers compared complete lesion curettage with suturing to selective curettage (40-70% lesion removal) with cyanoacrylate tissue adhesive closure to assess differences in healing and patient-related outcomes. Participants : Underwent endodontic microsurgery using one of the two surgical protocols Attended follow-up visits at 1, 3, and 7 days for clinical evaluation of pain, swelling ,Discomfort , Bleeding , Local reaction and Wound Dehiscence Attended follow-up visits at 3, 6, and 12 months for clinical and radiographic evaluation of periapical healing using 2D radiographs and CBCT
Trial Details
NCT Number NCT07353580
Lead Sponsor Mansoura University
Conditions Healing and Patient Related Outcomes
Enrollment 24 participants
Start Date 2024-12-25
Primary Completion 2026-01-29 (estimated)
Study Completion 2026-02-27 (estimated)
Updated on ClinicalTrials.gov 2026-01-20