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New imaging tool could sharpen spinal surgery precision

NCT ID NCT07416565

Diagnosis Sponsor: NYU Langone Health Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study will test a new imaging tool called the ATEC IntraOperative Alignment (IOA) Platform in 40 adults undergoing spinal deformity surgery. The tool helps surgeons see and measure spinal alignment during the operation, potentially allowing for more precise corrections. Researchers will compare its accuracy to standard X-rays and see how well it predicts final alignment after surgery.

What this could mean

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

Active substance
ATEC IntraOperative Alignment (IOA) Imaging Platform
What this could lead to
If successful, this tool could help surgeons make more accurate spinal corrections during surgery, potentially improving outcomes for patients with spinal deformities.
What could go wrong
This is a small, early-stage study with only 40 participants, so results may not apply to everyone. The tool is meant to assist, not replace, standard care, and its benefits over current methods are not yet proven.

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 40 people

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

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Aug 2029

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 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: 1. Skeletally mature patients 2. Able to give informed consent 3. Sagittal Spinal Deformity patients as defined by any of the following radiographic criteria: * Coronal cobb angle \>20 degrees * Pelvic Tilt \>25degrees * Sagittal Vertical Axis \>50mm * Pelvic Incidence - Lordosis of \>10 degrees * Thoracic Kyphosis \>60 degrees 4. Or clinically indicated for spinal fusion T10-Pelvis or more levels fused 5. Or adult degenerative pathology requiring 2 or more levels fused Exclusion Criteria: 1. Under the age of 18 years old 2. Skeletally immature patients 3. Active infection 4. Presence of inflammatory spinal disease (e.g. ankylosing spondylitis, Diffuse Idiopathic Skeletal Hyperostosis (DISH), Rheumatoid Arthritis) 5. Concurrent Spinal or pelvic fracture 6. Vulnerable patient (pregnant, prisoner, inability to consent)

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Spinal deformity

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

  • NYU Langone Health

    New York, New York, 10016, United States

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