Can sound waves dissolve fatty lumps without big scars?

NCT ID NCT07797270

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time

Summary

This trial tests whether a device called CUSA can remove lipomas, which are common benign fatty lumps under the skin, using a minimally invasive approach. Researchers plan to enroll 30 adults with lipomas larger than 1 cm on the trunk, limbs, or neck. The goal is to see if CUSA can completely remove the lipoma with smaller incisions, less scarring, and fewer recurrences compared to traditional open surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
CUSA, a minimally invasive surgical device that uses ultrasound to break up and remove lipomas
What this could lead to
If it works, this could offer a less invasive way to remove lipomas, with smaller scars, faster recovery, and lower recurrence rates than open surgery.
What could go wrong
This is a small, early-stage study with only 30 participants. The device may not fully remove the lipoma, and there is a risk of complications such as bleeding, infection, or recurrence.

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

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Jul 2028

An estimate. End dates often move.

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

18 to 60 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: 1\. Aged 18 to 60 years; 2. Subcutaneous lipoma confirmed by ultrasound and needle biopsy pathology; 3. Maximum diameter of the lipoma greater than 1 cm; 4. Lipoma located on the trunk, extremities, or neck (excluding the head and face); 5. Lipoma located in the subcutaneous fat layer with a safe distance from the skin and deep tissues; 6. Patients with explicit demand for minimally invasive and cosmetic treatment; 7. Voluntarily participate in the study and sign the informed consent form; 8. Willing to cooperate with preoperative examinations, intraoperative procedures, and postoperative follow-up. \- Exclusion Criteria: 1. Coagulation dysfunction or currently receiving anticoagulant therapy; 2. Lipoma located in the head and face or within the muscle layer; 3. Atypical lipoma or liposarcoma indicated by needle biopsy pathology; 4. Ulceration, redness, swelling, or infection of the skin overlying the lipoma; 5. Pregnant or lactating women; 6. Severe dysfunction of vital organs such as the heart, liver, or kidney; 7. Severe mental illness or cognitive impairment; 8. Previous history of surgery or radiotherapy at the same site; 9. Currently participating in other clinical studies. -

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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.

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