This study will evaluate the efficacy of abobotulinumtoxina on Veterans with post-traumatic headache
A significant proportion of headaches occur following head trauma, and therefore are referred to as post-traumatic headaches (PTH). Traumatic brain injury (TBI) is highly prevalent in the Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) population and consequently there has been a rise in PTH in the clinical setting at VA hospitals. Botulinum toxin type A (BoNT-A) has been shown to be effective in treating chronic migraine and chronic daily headache. It is therefore reasonable to predict that BoNT-A may also be effective in treating PTH. This study proposes that PTH and its associated symptoms may respond positively to BoNT-A treatment due to its similar pathophysiology and clinical resemblance to other headache disorders including tension type headache, typical migraine with or without aura, and chronic daily headache. Study Design: Veterans with mild, moderate or severe brain injury with a headache developing within 7 days after head trauma and persisting greater than 3 months were recruited from the Veterans Affairs Greater Los Angeles Healthcare System. The study is a prospective, double-blind, randomized, placebo-controlled, cross-over trial.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
Subjects were injected with 0.1 ml (12.5 units of Abobotulinumtoxina) into 31 distinct muscle locations in the head and neck
Subjects were injected with 0.1 ml of preservative free normal saline into 31 distinct muscle locations in the head and neck
VA Greater Los Angeles Healthcare System
Los Angeles, California, United States
Incidence of headaches from baseline
Evaluation in weekly incidence of headaches from baseline based on headache diary or weekly phone follow-up
Time frame: evaluation from time of injection until completion of 12 week follow-up
Intensity of headache pain
Evaluation of pain intensity using score of headache on Numerical Rating Scale (NRS) over time. The NRS is an 11-point scale for patient self-reporting of pain with 0 being no pain and 10 being the most severe pain.
Time frame: evaluation from time of injection until completion of 12 week follow-up
Number of headache days per week
Evaluation of the number of days a headache was present over each week
Time frame: evaluation from time of injection until completion of 12 week follow-up
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