Cupping vs. scraping: which eases back pain better?
NCT ID NCT07685340
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This study compares two non-drug treatments—dry dynamic cupping and instrument-assisted soft tissue mobilization (IASTM)—for people with chronic myofascial low back pain lasting more than three months. Over two weeks, participants receive three sessions per week of one therapy. Researchers measure changes in pain intensity, physical disability, and lower back mobility to see which approach offers greater relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dry dynamic cupping and instrument-assisted soft tissue mobilization
- What this could lead to
- If one method proves more effective, it could offer a better non-drug option for managing chronic low back pain.
- What could go wrong
- This is a small, early-stage comparison with only 48 participants, so results may not apply broadly. Both treatments are manual therapies with limited evidence.
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 48 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Sep 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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25 to 45 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: * Chronic Myofascial Lower Back Pain \> 3 months * Pain reproduced by palpation of Lumbar Para-Spinals, Quadratus Lumborum (QL) or Thoracolumbar Fascia. * Trigger Points will be diagnosed through Simons and Travell's Criteria * Age 25-45 years (young adults according to WHO classification) * Both genders Exclusion Criteria: * History of spinal surgery * Presence of inflammatory or neurological disorders * Facet joint dysfunction * Discogenic pain * Ligamentous pain * Pregnant females
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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
1 site. 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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Mediplex Healthcare Center, Rawalpindi
RECRUITINGRawalpindi, Punjab Province, 46000, Pakistan