Frozen shoulder: ultrasound gel or muscle exercises — which works better?
NCT ID NCT05475639
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This study compares two treatments for frozen shoulder (adhesive capsulitis): applying an anti-inflammatory gel through ultrasound (phonophoresis) versus a muscle relaxation exercise technique (post-isometric facilitation). About 45 adults aged 30–40 with the second stage of frozen shoulder will receive one of these treatments or standard physiotherapy three times a week for four weeks. Researchers will measure pain, pressure sensitivity, shoulder movement, and daily function to see which approach provides more relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Diclofenac gel (Voltaren) delivered via ultrasound
- What this could lead to
- If one treatment proves more effective, it could offer a simpler, drug-free option or a more targeted way to deliver pain relief for frozen shoulder.
- What could go wrong
- This is a small, early-stage study with only 45 participants, so results may not apply to everyone. Both treatments are generally safe but may not work for all cases.
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
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45 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Oct 2025
- Lead sponsor
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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
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30 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * The patient age will range from 30to 40years old from both sexes (male and female). * All recruited subjects in the 2nd stage of adhesive capsulitis (transitional stage). * The patient will be diagnosed and referred by orthopedist as Adhesive capsulitis. * The diagnosis will be confirmed by shoulder MRI. * The diagnosis will be confirmed by shrug test. * The patient will be referred by anterior shoulder pain or anterolateral shoulder pain. * Inclusion requirement include two or more of the following pain complaints: Grooming ones hair, Scratching your back and getting dressed, Overhead activities or Difficulty in the action of throwing the ball and giving a high -five. * All patients will sign the informed consent before joining the study. Exclusion Criteria: * Previous fracture with or without internal fixation in the shoulder joint * Any previous surgery in the shoulder joint and patient with tendon calcification * Local corticosteroid injection to the affected shoulder within the last three months or recent ones (Michener et al, 2004). * Neuromuscular disease * Rotator cuff tear * History of metastatic cancer or diagnosis of cancer within 12 months * Unstable angina
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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.
Contacts and locations
Locations
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Out patient clinic of faculty of physical therapy
Cairo, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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