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Surgeons reshape and plate lower ribs to flatten a bulging chest

NCT ID NCT07813234

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time

Summary

Researchers are studying a surgical procedure called anterior aesthetic rib cage remodeling with osteosynthesis (ARCO) in adults aged 18 to 45 with a prominent or misshapen lower rib cage. Through small incisions under the breast, surgeons cut the outer layer of ribs 6, 7, and 8, reshape them, and hold them in place with titanium plates and screws. The study tracks rib cage circumference, CT scans, breathing tests, chest appearance scores, and complications for 12 months to see whether the procedure reduces the lower rib bulge and how safe it is.

What this could mean

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

Active substance
a surgical procedure that reshapes and stabilizes the lower ribs with titanium plates
What this could lead to
If it works, this could offer adults with a prominent lower rib cage a surgical option to reduce the bulge and improve chest appearance.
What could go wrong
This is a single-group study with no comparison group, so any improvement cannot be clearly attributed to the surgery. Rib surgery carries risks such as collapsed lung, bleeding, infection, and problems with the plates or bone healing.

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.

Participants

About 160 people

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

Started

Jan 2025

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults seeking correction of anteroinferior rib cage prominence or deformity who meet the standardized ARCO operative criteria.

Ages

18 years and older

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: * Age 18 to 45 years, or older participants with documented acceptable bone health under the final protocol. * Prominence, dysmorphia, or contour concern involving the anteroinferior rib cage and judged appropriate for ARCO. * Preoperative chest CT, spirometry, medical history, and physical examination completed. * BMI 30 kg/m2 or lower. * Ability to comply with CT, spirometry, BODY-Q, and clinical follow-up through 12 months. * Written informed consent Exclusion Criteria: * Osteoarticular disease affecting rib integrity or clinically relevant osteoporosis risk. * Previous major chest surgery or significant thoracic trauma. * Coagulation disorder, chronic pulmonary disease, or uncontrolled systemic disease. * Active cancer, short life expectancy, or contraindication to elective surgery. * Known adverse reaction to the proposed osteosynthesis material. * Psychiatric condition or body-image disorder that, after specialist assessment when indicated, impairs informed decision-making or realistic expectations. * Pregnancy or breastfeeding.

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Clinica INO

    RECRUITING

    Bogotá, Colombia