Could ginger root ease sciatica pain? new study investigates
NCT ID NCT06817018
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether taking ginger root extract daily for 8 weeks can reduce pain and improve gut health in people with chronic sciatica. Researchers will measure pain levels, gut bacteria, and brain changes in 80 adults. The goal is to see if ginger affects the gut-brain connection to ease nerve pain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ginger root extract
- What this could lead to
- If it works, this could point toward a natural supplement to help manage chronic sciatica pain.
- What could go wrong
- This is a small, early-stage trial. The effect may be small or no better than placebo, and results may not apply to everyone with sciatica.
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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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Feb 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 85 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: * 18-85 years old men and women with BMI \< 25 or ≥ 30 kg/m2 * low back or gluteal pain radiating into leg(s) past the knee (sciatica) with pain duration of at least 3 months (chronic sciatica) * pain scale \> 3 out of 10 (0=no pain,10=worst pain imaginable) during the past 24 hours * willingness to accept randomization. * woman of childbearing potential agrees to use an effective form of contraception during the study Exclusion criteria: Sciatica aspects: * known or suspected serious spinal pathology (e.g., cauda equina syndrome or spinal fracture) * scheduled, or being considered, for spinal surgery or interventional procedures for sciatica during study period * focal neurological deficits with progressive or disabling symptoms * low back pain without sciatica GI aspects: * unstable GI disorder * history of chronic or systemic autoimmune diseases with GI involvement * recent (\<1 month) appearance of diarrhea or hematochezia before study begins * recent (\<1 month) exposure to antibiotics before study start Other exclusion considerations: * pregnant or breast-feeding women * women of child-bearing potential will have a urine pregnancy test done prior to the baseline MRI and administration of any study drug. The clinical research coordinator will run the pregnancy test and inform the patient of the results. If the test is positive, they will be withdrawn from study participation. * cognitive impairment, history of psychiatric conditions indicating mental health instability or incapacity * likeliness of moving during the trial, lack of transportation, or unavailability at sample collection times. * presence of a bleeding diathesis * taking anticoagulant medications (e.g Heparin, Warfarin) * taking dual antiplatelet medications (e.g. aspirin + Plavix) * participants with clinically significant laboratory abnormalities of liver function (AST and ALT) and kidney function (BUN and serum creatinine) abnormalities. Definition of clinically significant for liver function is AST/ALT ≥ 3.0x ULN and for kidney function is serum creatinine \> 2.0 mg/dl and BUN \> 1.5x ULN.
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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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Texas Tech University Health Sciences Center
NOT_YET_RECRUITINGLubbock, Texas, 79430, United States
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Texas Tech University Health Sciences Center
RECRUITINGLubbock, Texas, 79430, United States
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