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New dental material shows promise in root surgery Follow-Up

NCT ID NCT07254143

Knowledge-focused Sponsor: University of Medicine and Pharmacy at Ho Chi Minh City Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 16 adults who had root-end surgery (apicoectomy) using a material called MTA flow. The goal was to see if this material helps the tooth heal without pain, swelling, or infection within 6 months. Researchers checked X-rays and symptoms to measure success.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

16 people

The number who actually took part.

Started

Oct 2021

Finished

Dec 2022

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Study population are patients who came to Dental Department of 175 Military hospital for apical lesions.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * age 18 years or older * systemic health classified as I or II according to the American Society of Anesthesiologists (ASA) classification * willingness to participate in the study * failure of conventional or repeat endodontic treatment * a periapical lesion with a diameter ≥ 5 mm Exclusion Criteria: * a crown-to-root ratio ≥ 1.0 * inability to comply with the follow-up protocol

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Clinical and radiographic success in 6 months

Contacts and locations

Locations

  • Military Hospital 175

    Hanh Thong Ward, Ho Chi Minh City, 700000, Vietnam