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Can radiofrequency energy heal a painful shoulder tendon?

NCT ID NCT07794033

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 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 Results may not be published yet.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

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This status has not been confirmed recently, so it may be out of date.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 Aug 31, 2026 · Last updated Sep 02, 2026 · Updated 2 times

Summary

This trial tests whether TECAR therapy, which uses capacitive and resistive energy to heat deep tissues, can improve tendon thickness, reduce pain, and restore shoulder movement in people with supraspinatus tendinitis. Researchers will compare TECAR therapy to conventional physiotherapy in 50 adults aged 18 to 65 with chronic shoulder pain on their dominant side. The study measures changes in tendon thickness and subacromial space using ultrasound, along with pain, strength, and function. The goal is to see if this technology offers a better way to manage this common shoulder condition.

What this could mean

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

Active substance
TECAR therapy (capacitive and resistive energy transfer) compared with conventional physiotherapy
What this could lead to
If TECAR therapy works, it could offer a non-invasive option to reduce pain and improve shoulder function in people with supraspinatus tendinitis.
What could go wrong
This is a small, early-stage trial with 50 participants, so results may not apply broadly. TECAR therapy may not outperform standard physiotherapy, and individual responses can vary.

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.

Participants

About 50 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Apr 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.

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: 1. Fifty patients with chronic supraspinatus tendinitis on the dominant side. 2. Patients with age range from 18 to 65 years old from both genders. 3. Patients reporting positive empty can test. 4. patients reporting pain with resisted isometric abduction. 5. Patients experiencing shoulder pain for at least 4 weeks. 6. patients reporting pain with active shoulder elevation in the scapular plane. Exclusion Criteria: 1. Patients with shoulder surgery or trauma in the past 6 months will be excluded. 2. Patients with full-thickness rotator cuff tears, fractures, or severe osteoarthritis will be excluded. 3. Patients with systemic diseases affecting tendon healing (e.g., uncontrolled diabetes, rheumatoid arthritis) will be excluded. 4. Patients who were pregnant or breastfeeding will be excluded. 5. Patients currently receiving other shoulder therapies that could affect outcomes will be excluded. 6. Patients with frozen shoulder will be excluded. 7. Patients with glenohumeral or acromioclavicular arthritis will be excluded. 8. Patients with an implanted pacemaker will be excluded.

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Conditions

The condition(s) this trial relates to.

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

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    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

  • Shireen Mohamed Mahmoud

    Giza, 11432, Egypt