Shock wave therapy aims to ease stubborn back pain
NCT ID NCT07646132
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests two different doses of focal shock wave therapy in 60 adults with chronic low back pain lasting at least 12 weeks. Participants receive the treatment and are monitored for pain relief and improved daily function. The goal is to find which dosing works better for easing symptoms.
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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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2028
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 80 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: * Individuals of both sexes. * Age between 18 and 65 years. * Clinical diagnosis of mechanical chronic low back pain (cLBP), defined as pain localized between the lower costal margin and the gluteal fold, with at least 12 weeks of evolution. * Lumbar pain intensity of at least 5/10 on the Numeric Pain Rating Scale (NPRS). * Predominantly mechanical pain, exacerbated by activities such as prolonged standing, trunk movements, extension, or lumbar rotation, and without clinical data of predominant radicular pain. * Plain radiograph of the lumbar spine available as part of the baseline evaluation. * Ability to attend all 4 treatment sessions and subsequent follow-up evaluations. * Signed informed consent form previously approved by the Institutional Review Board / Research Ethics Committee. Exclusion Criteria: * Low back pain of probable non-mechanical origin or secondary to a specific cause that substantially modifies clinical management. * Clinical data of predominant lumbar radiculopathy, including pain radiating below the knee with a dermatomal distribution, focal motor deficit, objective sensory alterations, or compatible reflex changes. * Diagnosis or suspicion of cauda equina syndrome. * History of previous lumbar spine surgery. * Current vertebral fracture or recent history of lumbar fracture. * Spondylolisthesis grade II or higher. * Significant structural scoliosis or severe lumbar deformity that prevents treatment standardization. * Suspicion or evidence of a tumor, infection, spondylodiscitis, or axial inflammatory disease. * Severe clinically documented osteoporosis or history of vertebral fragility fracture. * Pregnancy or lactation. * Coagulation disorder, use of anticoagulants at therapeutic doses, or a hemorrhagic condition that increases procedure risk. * Previous epidural infiltration, facet block, radiofrequency, or other lumbar interventional procedure within a recent period defined by the protocol. * Current treatment with another physical rehabilitation modality or instrumental therapy directed at low back pain, if it cannot be suspended during the intervention period. * Current use of nonsteroidal anti-inflammatory drugs (NSAIDs) that the patient cannot suspend according to the study indications. * Concomitant neurological, rheumatological, oncological, or musculoskeletal disease that significantly interferes with pain or disability evaluation. * Cognitive impairment, decompensated psychiatric disorder, or any condition that prevents understanding instructions, answering questionnaires, or completing follow-up.
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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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Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde", Servicio de Medicina Física y Rehabilitación
Guadalajara, Jalisco, 44280, Mexico
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