Transnasal Sphenopalatine Ganglia Block for Management of Chronic Migraines in Pediatric Patients
Withdrawn before enrolling · Phase 2
Conditions studied: Migraine in Children, Pain, Neuropathic
In brief
Single-center, open-label, pre-post treatment pilot study to evaluate the safety and effectiveness of sphenopalatine ganglia blocks for the treatment of chronic migraine in the pediatric population. 50 children with a diagnosis of chronic migraines will undergo a series of three transnasal sphenopalatine ganglia blocks to measure their effect on headache frequency, headache intensity, headache duration, and use of headache medication.
Key facts
- Study ID
- NCT04466826
- Run by
- Washington University School of Medicine
- People needed
- 0
- Starts
- 2021-01-02
- Expected to finish
- 2021-02-05
- Last updated by the study team
- 2021-02-10
Who can join
Age: 8 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Children ages 8 to 17 years old Meet the criteria for chronic migraines Have remained stable on their current headache medication for a minimum of 4 weeks.
- Able to provide informed consent from parent or legal guardian Able to provide assent if subject is a minor of appropriate age
You may not qualify if…
- Allergy to local anesthetic Developmental delay (e.g. non-verbal) Inability to use numeric pain scale Inability to perform or tolerate transnasal procedure Substance abuse disorders Known pregnancy
Where it is running
- St. Louis Children's Hospital — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
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