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Which tube causes fewer nosebleeds in kids? study compares two options

NCT ID NCT06985108

Knowledge-focused Sponsor: Dicle University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at 98 children aged 3-18 having dental surgery under general anesthesia. Doctors compared a standard spiral breathing tube with a specially shaped nasal tube to see which caused fewer nosebleeds and was easier to insert. The goal is to find the safest way to place a breathing tube through the nose in children.

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

98 people

The number who actually took part.

Started

May 2025

Finished

Oct 2025

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

3 to 18 years

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: * Being between 3-18 years old * No anomaly preventing nasal intubation * To be in ASA1-2 classification according to ASA criteria Exclusion Criteria: * Lack of consent of the patient/ relatives * Facial anomaly that prevents nasal intubation * Being in the ASA3-4 group according to ASA criteria

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Conditions

The condition(s) this trial relates to.

Epistaxis

As listed by the trial registrant

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

Epistaxis

Contacts and locations

Locations

  • Dicle university Faculty of dentistry

    Diyarbakır, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.