Acupuncture may ease chronic pain in spinal cord injury
NCT ID NCT03197675
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This trial investigates whether acupuncture can reduce pain and improve function in people with spinal cord injury. Participants receive either acupuncture with electrical stimulation plus ear acupuncture, or standard care alone, for eight weeks. The study measures pain levels, quality of life, and functional recovery over three months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- acupuncture with electrical stimulation and auricular acupuncture
- What this could lead to
- If effective, acupuncture could offer a drug-free option to manage chronic pain and improve quality of life for people with spinal cord injury.
- What could go wrong
- This is a mid-stage trial with a moderate number of participants. Previous studies have shown mixed results, and the effect may be small or not lasting.
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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69 people
The number who actually took part.
- Started
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Mar 2018
- Finished
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Feb 2023
- 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 75 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: 1. age between 18 and 75 2. complete (AIS A) or incomplete SCI (AIS B-D) of the cervical, thoracic or lumbar spine from blunt or penetrating trauma 3. ability to understand verbal and written English Exclusion Criteria: 1. a history of peripheral neuropathy 2. medical diagnoses or conditions that preclude them from active participation (for example, moderate or severe traumatic brain injury) 3. receipt of acupuncture in the last three months prior to enrollment 4. presence of skin breakdown or infection over the extremities or external ears 5. active participation in other research studies 6. cognitive impairment that prevents understanding the test instructions 7. prisoner 8. pregnancy 9. active duty military personnel 10. individuals who do not speak or understand the English language
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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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R Adams Cowley Shock Trauma Center, University of Maryland Medical Center
Baltimore, Maryland, 21201, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Early detrusor chemodenervation to preserve bladder compliance and longevity after spinal cord injury
- Prevention of thromboembolism using apixaban vs enoxaparin following spinal cord injury
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