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PRP injection shows promise for shoulder tendon healing

NCT ID NCT07456215

Disease control Sponsor: Aristotle University Of Thessaloniki 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether platelet-rich plasma (PRP) can improve tendon healing in people with a torn rotator cuff. Forty adults having arthroscopic repair surgery were split into two groups: one received PRP during surgery, the other did not. Researchers compared tendon tissue samples to see if PRP led to better structure and cell health.

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

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

40 people

The number who actually took part.

Started

Dec 2022

Finished

Jan 2026

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

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: * Full thickness rotator cuff tear treated with arthroscopic repair * Age of 18 to 65 years * Chronic shoulder pain due to rotator cuff tear * Magnetic resonance imaging study within 6 months prior to arthroscopy * Goutallier grade 1 or 2 muscle fatty infiltration Exclusion Criteria: * Comorbidities, including coagulopathy, liver disease, cancer, nutritional disorder * Goutallier grade 3 or 4 muscle fatty infiltration * Shoulder osteoarthritis, rotator cuff arthropathy, rheumatoid arthritis * History oof shoulder injection within the last 12 months * History of prior shoulder surgery

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Conditions

The condition(s) this trial relates to.

disease of the tendon familial pityriasis rubra pilaris rotator cuff syndrome Tendon Injuries

As listed by the trial registrant

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

PRP Supraspinatus injury Tendon injuries

Contacts and locations

Locations

  • Charalampos Pitsilos

    Thessaloniki, Cental Macedonia, 54635, Greece

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