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Shoulder MRI study pulled before starting

NCT ID NCT06043791

Knowledge-focused Sponsor: Henry Ford Health System 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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 was designed to see if a stronger MRI machine (3 Tesla) without contrast dye could find shoulder labral tears as well as the current standard MRI with contrast. Researchers planned to enroll adults aged 18-65 who were likely to need shoulder surgery. However, the study was withdrawn before any participants were enrolled, so no results are available.

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.

Expected to start

Sep 2025

An estimate. Start dates often move.

Expected to finish

Sep 2026

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 65 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: * Indicated for likely labral surgery * Chronic, degenerative labral and/or cartilage pathology * Ability to read and understand English * Age ≥ 18 years * Age ≤ 65 years Exclusion Criteria: * Patient does not complete both the MR arthrogram and 3T non-contrast MRI * Unexpected trauma in between the MR arthrogram and 3T non-contrast MRI * Age \< 18 years * Age \> 65 years

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Conditions

The condition(s) this trial relates to.

Rotator Cuff Injuries

As listed by the trial registrant

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

Labral tear, glenoid

Contacts and locations

Locations

  • Henry Ford Health

    Royal Oak, Michigan, 48067, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.