Braces study measures tooth blood flow to improve safety
NCT ID NCT07630818
First seen Jun 26, 2026 · Last updated Sep 11, 2026 · Updated 5 times
Summary
This study looked at how applying orthodontic force (about 150g) to teeth affects oxygen levels in the tooth pulp. Researchers used CBCT scans and a special pulse oximeter on 35 patients aged 15-35 undergoing braces treatment. The goal was to understand how tooth anatomy and force influence pulp health, which could help make orthodontic treatment safer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help orthodontists apply braces more safely by understanding how tooth pressure affects blood flow.
- What could go wrong
- This is a small, completed observational study with only 35 participants. It does not test a treatment, so findings may not change practice directly.
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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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38 people
The number who actually took part.
- Started
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May 2025
- Finished
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Sep 2026
- 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 35 years
- Sex
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Anyone
- Healthy volunteers
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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: * Patients aged between 15 and 35 years old. * Patients undergoing routine fixed orthodontic treatment with indications for premolar extractions and subsequent canine retraction phase. * Target canines must be vital with healthy dental pulp and no periapical pathology. * Pre-existing Cone-Beam Computed Tomography (CBCT) scans of acceptable diagnostic quality available in the patient's records, taken prior to the canine retraction phase. * Patient or legal guardian provides written informed consent to participate in the study. Exclusion Criteria: * Target canines with a history of dental trauma, extensive caries, periodontal disease, or previous endodontic treatment. * Patients with systemic diseases affecting peripheral blood circulation or microvasculature (e.g., cardiovascular diseases, severe anemia, diabetes, chronic respiratory conditions). * Patients currently using systemic vasoconstrictors or anti-inflammatory medications during the active monitoring period. * Pregnancy or lactation. * Refusal to sign the informed consent form.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Can Tho University of Medicine and Pharmacy
Can Tho, 900000, Vietnam
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