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New 3D scanner aims to make spine surgery more precise

NCT ID NCT06267248

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
Registered, but not yet taking participants.
By invitation only This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 early study tests a new 3D scanner that takes pictures of the spine during surgery. The goal is to see if the scanner can accurately match these pictures to MRI or CT scans taken before or during the operation. Ten patients having spine surgery will participate. The study focuses on how well the device works and how surgeons use it, not on treating a disease.

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 10 people

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

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Nov 2028

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

Subjects will be invited to participate from the Principal Investigator's clinic population. All subjects will be identified as requiring a spine surgery that meets the eligibility requirements.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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. Patients that require exposure of posterior bony anatomy for visualization as standard of care. 2. Patients will have had a CT scan performed prior to the procedure as standard of care, or is expected to have a CT scan intraoperatively as standard of care. 3. Clinically planned for spine surgery. 4. Able to provide written informed consent from subject, using IRB approved consent form and agrees to comply with protocol requirements. 5. Patients who do not speak English will be allowed to participate, with the expectation that the site will provide interpreter services to help with the consent process. Exclusion Criteria: 1. Language problems that would prevent from properly understanding instructions in any language. 2. Patients less than 18 years of age or older than 80 years of age 3. Patients who are excluded from consideration for the surgical procedure are therefore excluded from the research study. 4. Special populations: pregnant women, prisoners. 5. Minimally invasive spine surgery that does not expose the necessary bone/s. 6. Spine surgery without posterior exposure. 7. Patients considered high risk for anesthesia, as determined by operative surgeon

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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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • Mass General Bringham, Hale Building for Transformative Medicine

    Boston, Massachusetts, 02115, United States

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