Zapping cartilage with radio waves could reshape noses without extra cuts
NCT ID NCT07032675
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a low-temperature radiofrequency device can reshape nose or ear cartilage during surgery to improve breathing and appearance. Twenty adults having septorhinoplasty will have their cartilage reshaped with the device before reimplantation. Researchers will measure how many treatments are needed, changes in shape, and patient satisfaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low-temperature radiofrequency device (Vivaer)
- What this could lead to
- If successful, this technique could offer a less invasive way to reshape cartilage during nose surgery, potentially improving both breathing and cosmetic results.
- What could go wrong
- This is a very small early study (20 people) testing cartilage reshaping outside the body. It may not translate to better outcomes in actual patients, and the procedure could still require additional treatments or cause side effects.
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 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jun 2027
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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18 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: • Patients 18 years and older undergoing functional septorhinoplasty or cosmetic septorhinoplasty, with or without auricular cartilage harvest Exclusion Criteria: * Patients who have had a prior septorhinoplasty * Patients who have received prior head and neck radiation * Patients with a septal perforation * Patients who are medically ineligible to undergo septorhinoplasty.
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Get notified about this study
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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
6 sites. 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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IU Health Methodist Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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IU Health North Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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IU Health Saxony Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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IU Health University Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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IU Health West Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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Riley Hospital for Children at IU Health
RECRUITINGIndianapolis, Indiana, 46202, United States