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Shoulder surgery secrets: anchor angle may determine healing success

NCT ID NCT07661680

Knowledge-focused Sponsor: Fatih Sultan Mehmet Training and Research Hospital 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 10, 2026 · Updated 4 times

Summary

This study looks at how the position and angle of surgical anchors used in rotator cuff repair affect cyst formation and tendon healing. Researchers will use MRI scans to measure cyst volume and assess tendon recovery in 70 adults aged 18–70 undergoing primary arthroscopic repair. The goal is to identify surgical factors that lead to better shoulder function and fewer complications.

What this could mean

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

What this could lead to
If clear links are found, surgeons may adjust anchor placement to reduce cyst formation and improve tendon healing after rotator cuff repair.
What could go wrong
This is an observational study, not a treatment trial. It may not prove that anchor parameters directly cause better outcomes, and results may not apply to all patients.

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 70 people

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

Started

May 2026

Expected to finish

Aug 2027

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.

Who is studied

The study will include patients with: * Partial- or full-thickness rotator cuff tears * Indication for surgical repair based on clinical and imaging findings * Ability to comply with postoperative follow-up and MRI evaluation The population is expected to represent a typical rotator cuff repair cohort in daily clinical practice.

Ages

18 to 70 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: * Age 18-70 years * Undergoing primary arthoroscopic rotator cuff repair * Availability for MRI follow-up * Ability to provide informed constent Exclusion Criteria: * Previous shoulder surgery * Active infection * Inflammatory joint disease * Acute traumatic massive tears * Inability to complete follow-up

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Conditions

The condition(s) this trial relates to.

disease of the tendon Muscle Weakness Rotator Cuff Injuries rotator cuff syndrome Tendon Injuries

As listed by the trial registrant

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

Muscle weakness Rotator cuff tears Tendon injuries Tendon thickening

Contacts and locations

Locations

  • Istanbul Provincial Health Directorate Fatih Sultan Mehmet Training and Research Hospital

    Istanbul, 340000, Turkey (Türkiye)

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