Could adding cupping to acupuncture double shoulder pain relief?
NCT ID NCT07545785
First seen Jun 27, 2026 · Last updated Aug 11, 2026 · Updated 2 times
Summary
This study tests whether combining electroacupuncture with vacuum cupping therapy works better than electroacupuncture alone for shoulder tendinitis. Fifty-four adults with shoulder pain and stiffness will receive either electroacupuncture alone or electroacupuncture plus cupping over two weeks. Researchers will measure pain, disability, and range of motion to see if the combo treatment offers extra relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- electroacupuncture and vacuum cupping therapy
- What this could lead to
- If it works, this could point toward a more effective non-drug treatment for shoulder tendinitis pain and stiffness.
- What could go wrong
- This is a small, early-stage trial with only 54 participants and a short two-week follow-up. The results may not apply to everyone, and the added benefit of cupping is uncertain.
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
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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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About 54 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- 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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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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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 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: * Patients between 18 and 70 years old. * Pain intensity score on the Visual Analogue Scale (VAS) between 4 and 7. * Diagnosis of rotator cuff and/or long head of the biceps tendonitis according to the guidelines issued by the Ministry of Health of Vietnam. * Mechanical pain that increases during movements such as abduction or raising the arm. * Presence of tender points at the long head of the biceps tendon or supraspinatus tendon . * Pain that increases during resisted contraction tests, such as the Jobe test or Palm-up test. * Absence of limitation in the passive range of motion of the shoulder. * Ultrasound findings showing a hypoechoic tendon or evidence of calcification. * Absence of motor weakness or paralysis. * Diagnosis of the TCM syndrome "Qi Stagnation and Blood Stasis" Exclusion Criteria: * Patients who do not agree to participate in the study. * Diagnosis of pseudo-paralysis, acute calcific periarthritis, or frozen shoulder. * Shoulder pain caused by cervical nerve root lesions. * Shoulder pain originating from apical lung tumors, coronary artery disease, or myocardial infarction. * Specific joint lesions caused by infection, tuberculosis, or rheumatoid arthritis. * Bone pathologies including fractures, dislocations, or osteonecrosis of the humeral head. * Shoulder dysfunction resulting from stroke or hemiplegia. * Women who are pregnant. * Patients with mental illness. * Contraindications for vacuum cupping, such as acute skin inflammation, open wounds, or alcohol consumption. * Contraindications for electroacupuncture, including cardiac pacemakers, heart failure, or local skin ulcers. * Current participation in another intervention study. * Use of painkillers, muscle relaxants, or within the last week. * Use of anticoagulants or a history of hemophilia.
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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.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Ho Chi Minh City Orthopedics and Rehabilitation Hospital
RECRUITINGHo Chi Minh City, 72121, Vietnam
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Le Van Thinh Hospital
RECRUITINGHo Chi Minh City, 71322, Vietnam
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