Braces breakthrough? simple wire stopper may replace screws in orthodontics
NCT ID NCT06416904
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a simple arch wire stopper can control molar movement as well as mini-screws during canine retraction in 26 post-pubertal female patients with dental protrusion. The goal was to see which method better prevents unwanted tooth movement. The trial is complete, but results are not yet widely available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- arch wire stopper and mini-screw (devices)
- What this could lead to
- If successful, this could show that a simpler, less invasive device (arch wire stopper) works as well as mini-screws for controlling tooth movement during orthodontic treatment.
- What could go wrong
- This is a small, completed trial with only 26 participants, so results may not apply to all patients. The devices are for temporary use during treatment and do not address underlying dental issues.
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
-
26 people
The number who actually took part.
- Started
-
Feb 2024
- Finished
-
Dec 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
-
15 to 25 years
- Sex
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Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Post-pubertal female patients. * Cases with bimaxillary protrusion or Class II Division 1 malocclusion that require maxillary first premolars extraction. * Full permanent dentition (not necessitating third molars). * Good oral hygiene. Exclusion Criteria: * Medically compromised patients. * Active periodontal disease or obvious bone loss in the maxillary arch. * Patients with habits that are detrimental to dental occlusion (thumb sucking, tongue thrusting). * Smoking or any systemic diseases. * Chronic use of any medications including antibiotics, phenytoin, cyclosporine, anti-inflammatory drugs, systemic corticosteroids, and calcium channel blockers. All the above factors affect the rate of tooth movement * Previous orthodontic treatment. * Missing teeth.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Faculty of Dentistry, Cairo University
Cairo, 12613, Egypt
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Other studies related to the condition(s) this trial covers.
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