Clear aligners take on braces in overbite showdown
NCT ID NCT05684510
First seen Jun 25, 2026 · Last updated Sep 17, 2026 · Updated 3 times
Summary
This study tests whether clear aligners with rubber bands can correct a mild overbite (Class II malocclusion) as well as traditional braces. Twenty-four people aged 15-20 will be randomly assigned to either clear aligners or braces, both with elastics. Researchers will measure changes in jaw position and tooth alignment using X-rays.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- clear aligners with intermaxillary elastics
- What this could lead to
- If successful, this could show that clear aligners are as effective as braces for correcting mild overbite, offering a more comfortable and less visible treatment option.
- What could go wrong
- This is a small, early-stage trial with only 24 participants, so results may not apply to everyone. The study measures bone and tooth changes, not long-term stability or patient satisfaction.
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
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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
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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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15 to 20 years
- Sex
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Anyone
- Healthy volunteers
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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 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: * \- Patients with permanent occlusion at age 15-20 years. * Patients with class II division I (half cusp or Less) with moderate overjet (2-4mm). * Patients with normal or horizontal growth pattern. * Mild crowding (\_\<2 mm) in maxillary and mandibular arch. * Patient with satisfactory periodontal health and good oral hygiene * No previous orthodontic treatment * Comprehensive medical and dental history ruling out any systemic disease. Exclusion Criteria: * Patients with periodontal disease. * Patients with vertical growth pattern. * Patients with missing or extracted teeth except third molar. * Patients with temporomandibular joint disorder. * Patients with Skeletal open bite. * Patients with poor oral and gingival health * Patients with neuromuscular disorder. * Patients with severe skeletal class II.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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Hama University
RECRUITINGHama, Hama Governorate, Syria
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Other studies related to the condition(s) this trial covers.
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