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CompletedNCT07877168Updated Oct 16, 2026

Clinical and Radiographic Healing After Microscope-Assisted Endodontic Surgery

An interventional study of Microscope-Assisted Endodontic Surgery in Periapical Lesions, sponsored by University of Medicine and Pharmacy at Ho Chi Minh City. Completed at 2 sites in Vietnam. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by University of Medicine and Pharmacy at Ho Chi Minh City · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 2 months after the study started (first participant enrolled Jul 2024, registered Oct 2026).
Updated Oct 16, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This study aimed to evaluate clinical and periapical radiographic healing following endodontic surgery using a surgical microscope.

An uncontrolled longitudinal clinical intervention study was conducted in patients requiring endodontic surgery. All surgical procedures were performed using a surgical microscope, ultrasonic instruments, and mineral trioxide aggregate (MTA) root-end filling.

Postoperative healing was evaluated through clinical examinations and periapical radiographs at scheduled follow-up visits over a 3-month period. The study assessed clinical healing, radiographic healing, changes in periapical radiolucency, and overall treatment success.

02

Conditions studied

  • Periapical Lesions

Keywords

  • Endodontic Surgery
  • Surgical Microscope
  • Periapical Healing
  • Mineral Trioxide Aggregate (MTA)
03

In context

Lead sponsor

University of Medicine and Pharmacy at Ho Chi Minh City is the lead sponsor of 121 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients classified as ASA I-II.
  • Patients who agreed to participate and were willing to provide information and attend scheduled follow-up visits.
  • Teeth indicated for endodontic surgery and considered preservable and restorable.

Exclusion criteria

Exclusion Criteria:

  • Patients with contraindications to oral surgery.
  • Teeth with extensive destruction of dental and surrounding periodontal tissues, severe bone loss, or nonrestorable crowns.
  • Periapical lesions with radiographic features suggestive of a tumor or malignancy.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    Microscope-Assisted Endodontic Surgery

    All participants underwent microscope-assisted endodontic surgery for teeth with periapical lesions and were followed for 3 months to assess clinical and radiographic healing.

    Procedure: Microscope-Assisted Endodontic Surgery

Interventions

  • ProcedureMicroscope-Assisted Endodontic Surgery

    Endodontic surgery was performed under a surgical microscope. The procedure included flap elevation, ultrasonic osteotomy, removal of periapical inflammatory tissue, resection of the apical 3 mm of the root, ultrasonic preparation of a 3-mm-deep root-end cavity, and root-end filling with MTA Repair HP. The surgical flap was repositioned and sutured.

06

What researchers measure

Primary outcomes

  1. Clinical Healing

    Clinical healing was assessed according to the criteria of Gutmann and Harrison (1994) and classified into three categories: complete, uncertain, and unsatisfactory healing. Complete healing was defined as the absence of pain, infection, swelling, sinus tract, tenderness on palpation or percussion, tooth mobility, periodontal pocket communication with the root apex, and adverse effects on adjacent teeth. Uncertain healing was defined by at least one of the following: vague intermittent symptoms, pressure or swelling sensation at the surgical site, mild pain on palpation, percussion, or chewing, or discomfort when applying pressure with the tongue. Unsatisfactory healing was defined by at least one of the following: severe pain, infection, swelling, sinus tract, severe tenderness on palpation or percussion, tooth mobility, periodontal pocket communication with the root apex, or adverse effects on adjacent teeth.

    Time frame: 1 and 3 months after surgery

  2. Radiographic Healing

    Periapical radiographic healing was assessed using study-defined criteria based on Rud (1972) and Molven (1987). Three components were evaluated: the apical periodontal ligament space and lamina dura, periapical radiolucency, and bone regeneration. Healing was classified as complete (restoration of a continuous lamina dura and complete bone regeneration), incomplete (reduced radiolucency with bone regeneration, irregular margins, and an asymmetric radiolucency separated from the periodontal ligament space), uncertain (reduced, round or semicircular radiolucency continuous with the periodontal ligament space), or unsatisfactory (unchanged or increased radiolucency). Complete healing required all three components to be complete; incomplete healing required at least one incomplete component with all others complete; uncertain healing required at least one uncertain component and no unsatisfactory component; and unsatisfactory healing required at least one unsatisfactory component.

    Time frame: 1 and 3 months after surgery

07

Study locations

2 sites
  • Center of Dentistry, University of Medicine and Pharmacy at Ho Chi Minh City
    Ho Chi Minh City, 70000, Vietnam
  • Ho Chi Minh City Odonto-Stomatology Hospital
    Ho Chi Minh City, 70000, Vietnam
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2024 to primary completion in Jul 2025, 12 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 9, 2026
First posted
Oct 16, 2026
StartActual
Jul 28, 2024
Primary completionActual
Jul 31, 2025
CompletionActual
Jul 31, 2025
Last update
Oct 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07877168
Responsible party
Le Huynh Thien An (Lecturer, Faculty of Dentistry, University of Medicine and Pharmacy at Ho Chi Minh City) — Principal investigator
First posted
Oct 16, 2026
Start date
Jul 28, 2024
Primary completion
Jul 31, 2025
Completion
Jul 31, 2025
Last update
Oct 16, 2026

Study contacts

Huynh Thien An Le, PhD
principal investigator · University of Medicine and Pharmacy at Ho Chi Minh City

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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