Phase
Condition
Pain (Pediatric)
Pain
Chronic Pain
Treatment
Methylprednisolone
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Provision of signed and dated informed consent form (in person or via telehealth)
Stated willingness to comply with all study procedures and availability for theduration of the study
Male or female, aged >18 years old
Ability to take oral medication and be willing to adhere to the study regimen asdescribed in this protocol
Patients presenting with all types of post-concussive headache with >5/10 inseverity on the numerical analog scale.
Headache that occurs for > 4 hours per day
Headache that occurs every day
Headache that began after concussion, patient was diagnosed at an outpatient clinicor was hospitalized
Headache developed within 7 days post-injury and patient presenting within 30 daysfrom initial trauma
A diagnosis of concussion.
If a patient is taking another pain medication, this still be included in the stud
Exclusion
Exclusion Criteria:
Any evidence of known intracranial hemorrhage on neuroimaging
Headache developing after 7 days post injury and patient presenting after 30 daysfrom initial trauma
Headache occurs < 4 hours per day
Headache does not occur daily
Age < or = 18
Headache is < 5 in severity on numerical analog scale
Presence of increase in intracranial pressure or papilledema
Any contraindication to corticosteroids
Allergy or sensitivity to corticosteroids
Active Tuberculosis
Active pregnancy
Currently on corticosteroids for another reason
Participants with fungal infection
Study Design
Study Description
Connect with a study center
Northwell Health - North Shore University Hospital
Manhasset, New York 11030
United StatesActive - Recruiting
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