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NCT Number: NCT07353580

Selective Curettage and Tissue Adhesive in Endodontic Microsurgery

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

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Dentisrty , Mansoura University

Al Mansurah, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years and older consenting to the surgical procedure as well as agreeing to preoperative and at least 1 follow-up CBCT evaluation.
  • Noncontributory medical history (American Society of Anesthesiologists class I, II).
  • Teeth with periapical lesions that had been previously treated or retreated but symptoms persist or recurrent.
  • Radiographic presence of true endodontic lesion close to vital critical structure.

Exclusion criteria

  • Nonconsenting patients and patients younger than 18 years of age.
  • Medical history with the American Society of Anesthesiologists class III to V.
  • Insufficient coronal restoration.
  • Nonrestorability or traumatized teeth.
  • Mobility > 1.
  • Vertical root fracture.

Treatment and study plan

Selective Lesion Curettage and Cyanoacrylate Tissue Adhesive

Procedure

Selective curettage is a conservative approach to treat periapical lesions by removing part of the granulomatous tissue while avoiding complications and damage to the neighboring structures. It also provides the least traumatic approach with minimal post-operative complications. It had an additional advantage, which is providing tissue samples for biopsy of the lesion, especially in cases where there was a diagnostic dilemma regarding its origin . In the selective curettage technique, approximately 50-70% of the granulomatous tissue was removed while preserving the portion in close proximity to critical areas, followed by standard root-end resection and retrofilling then Clinical and radiographic assessments, including CBCT, for bone healing assesment .

Complete Periapical Lesion Curettage and Suturing

Procedure

Complete Periapical Lesion Curettage and Suturing is a conventional endodontic microsurgical procedure performed to manage persistent periapical pathology following root canal treatment. After administration of local anesthesia, a full-thickness mucoperiosteal flap is elevated to expose the periapical region. The periapical lesion is completely curetted and removed, followed by apical root-end resection. A retrograde cavity is prepared using ultrasonic tips and sealed with a biocompatible root-end filling material. Hemostasis is achieved, and the surgical flap is repositioned and stabilized using conventional sutures. This approach represents the standard surgical protocol for endodontic microsurgery and serves as the active comparator in this study.

Primary outcomes

  1. Pain intensity

    Time frame: (1st, 3rd, and 7th day post-operative)

    Pain intensity is assessed using the Visual Analogue Scale (VAS, 0-10)

  2. Swelling

    Time frame: 1st, 3rd, and 7th day post-operative

    Presence of swelling is assessed clinically by visual inspection and physical examination and recorded as a binary outcome (present / absent)

Secondary outcomes

  1. Bleeding

    Time frame: 1st, 3rd, and 7th day post-operative

    Post-operative bleeding presence is assessed as a binary outcome (Yes / No)

  2. Radiographic Bone healing

    Time frame: 3, 6 , and 12 months

    Radiographic bone healing is assessed using standardized periapical radiographs (2D) and cone beam computed tomography (CBCT, 3D)

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Impact of Selective Curettage and Tissue Adhesive on the Clinical Outcomes of Endodontic Microsurgery: A Randomized Controlled Trial

Acronym: Microsurgery

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jan 20, 2026
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.