Shoulder pain relief without surgery? hyaluronic acid injections under study

NCT ID NCT07699406

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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 Results may not be published yet.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

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Status unknown
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First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time

Summary

This study investigates whether ultrasound-guided injections of low-molecular-weight hyaluronic acid (Hyalotend®) can safely reduce pain and improve shoulder function in people with chronic non-calcific supraspinatus tendinopathy. Participants receive two injections and are followed over time to track changes in pain, daily activities, and any side effects. The goal is to see if this treatment offers a non-surgical option for those who haven't found relief with physical therapy or medication.

What this could mean

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

Active substance
Low-molecular-weight hyaluronic acid (Hyalotend®)
What this could lead to
If successful, this approach could offer a non-surgical treatment option for chronic shoulder tendon pain that hasn't improved with physical therapy or medication.
What could go wrong
This is a small, single-arm observational study with only 30 participants, so results may not apply broadly. The treatment may not provide lasting relief, and injection-related side effects are possible.

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 30 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Mar 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

Patients will be recruited from the outpatient clinics of the Department of Physical Medicine and Rehabilitation at Hospital Universitario Nuestra Señora de Candelaria. Eligible participants will be patients referred to the department because of shoulder pain and/or impaired shoulder function. The diagnosis of chronic supraspinatus tendinopathy will be established by a rehabilitation physician based on the patient's medical history, physical examination, and ultrasound assessment, while excluding the presence of tendon calcifications and partial- or full-thickness tendon tears.

Ages

18 years and older

Sex

Anyone

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 years. * Clinical and ultrasound-confirmed diagnosis of chronic (\>12 weeks) supraspinatus tendinopathy. * No structural tendon tear, confirmed by ultrasound. * No tendon calcification, confirmed by ultrasound. * Previous failure of conservative treatment, including physical therapy and/or analgesic or anti-inflammatory medication. * Written informed consent provided. Exclusion Criteria: * Partial- or full-thickness supraspinatus tendon tear identified by ultrasound. * Calcific supraspinatus tendinopathy identified by ultrasound. * Subacromial-subdeltoid bursitis identified by ultrasound * Previous treatment with extracorporeal focus shock wave therapy within the last 3 months. * Previous corticosteroid or platelet-rich plasma (PRP) injection within the last 3 months. * History of hypersensitivity or allergy to hyaluronic acid or any of its components. * Uncontrolled systemic disease. * Other chronic rheumatologic or autoimmune diseases. * Pregnancy or breastfeeding.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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How to take part

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  1. The official record

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