Laser frenectomy pain in kids: which scale tells the truth?

NCT ID NCT07706023

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time

Summary

This study tracks pain levels in children aged 8 to 14 after a laser-assisted frenectomy, a procedure to correct a tight lip or tongue tie. For seven days after surgery, kids rate their pain using three different scales, including emoji and face-based tools. The goal is to find which scale works best for measuring pain in children and to understand how pain changes over the first week.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
diode laser-assisted frenectomy
What this could lead to
If successful, this study could help identify the most reliable way to measure pain in children after minor oral surgery, improving comfort and care.
What could go wrong
This is a small, single-group study without a comparison group, so results may not apply to all children or settings. Pain scales are subjective and may vary.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 53 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

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.

Ages

8 to 14 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Children aged 8 to 14 years. * Patients requiring diode laser-assisted frenectomy based on clinical indication. * American Society of Anesthesiologists (ASA) Physical Status I or II. * Ability of the participant and parent/legal guardian to understand the study procedures. * Written informed consent obtained from the parent or legal guardian, with assent obtained from the child when appropriate. Exclusion Criteria: * Presence of systemic diseases or medical conditions that could influence wound healing or pain perception. * Current use of analgesic, anti-inflammatory, corticosteroid, or psychotropic medications. * History of allergy or contraindication to local anesthetic agents. * Acute oral infection at the surgical site. * Previous oral soft tissue surgery in the same anatomical region. * Inability or unwillingness to complete the postoperative pain assessment forms for seven consecutive days. * Withdrawal of consent at any time during the study.

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Afyonkarahisar Health Science University

    Afyonkarahisar, 03300, Turkey (Türkiye)

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