Nerve block offers hope for migraine sufferers Who've tried everything
NCT ID NCT06891118
First seen Jun 27, 2026 · Last updated Sep 10, 2026 · Updated 4 times
Summary
This study tested a nerve block called a stellate ganglion block for people with chronic migraine that didn't get better with other treatments. 42 patients received the injection under ultrasound guidance. Researchers tracked changes in monthly headache days and pain scores over 6 months to see if the procedure helped.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stellate ganglion block (nerve block injection)
- What this could lead to
- If effective, this nerve block could offer a new option for people with chronic migraine who haven't found relief from standard treatments.
- What could go wrong
- This is a small, single-center study with no control group, so results may not apply widely. The procedure carries risks like bleeding, infection, or nerve damage.
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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42 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Dec 2025
- 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 65 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Adults aged 18-65 years. * Diagnosis of chronic migraine according to ICHD-3 criteria. * Insufficient clinical response to prior preventive migraine treatment. * Prior interventional headache treatment performed at least 3 months before enrollment, with insufficient clinical benefit. * Willingness and ability to participate in the study, comply with follow-up, and undergo the planned interventional treatment. Exclusion Criteria * History of a primary headache disorder other than migraine. * Migraine-related interventional treatment, botulinum toxin A treatment, or nonpharmacological headache treatment (e.g., acupuncture, ozone therapy, or cognitive behavioral therapy) within the previous 3 months. * Infection at the planned injection site. * Pregnancy or suspected pregnancy. * Known allergy to local anesthetic agents. * History of malignancy or cranial/cervical surgery. * Bleeding or coagulation disorder, or current oral anticoagulant therapy. * Comorbid conditions that could contribute to headache, such as uncontrolled hypertension or intracranial lesions. * Conditions that could impair adherence to the treatment or follow-up protocol, such as significant psychiatric disease or dementia. * Unwillingness to undergo the planned interventional treatment or to continue the study protocol.
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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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Health Sciences University, Ankara Bilkent City Hospital
Ankara, Cankaya, 06800, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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