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The primary objective of this study is to evaluate the efficacy of the Avulux device in reducing the impact of migraine headaches as measured by improvement in Headache Impact Test (HIT-6TM) scores at three weeks when compared to a control/sham device.
Full description
Avulux™ is intended to decrease the impact of headache and migraine on normal daily life and the ability to function, and reduce the frequency and severity of headache, in adult patients diagnosed with episodic migraine headache or chronic migraine.
Avulux™ consists of a pair of optical filters in the form of spectacle lenses, provided in standard spectacle frames or as clip-on units, coated with a thin film that effectively blocks light at specified wavelength ranges while minimizing distortion of the visible spectrum. The optical filters block a portion of the optical spectrum that is suspected to stimulate photophobic responses that trigger some, and exacerbate most, migraines.
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Inclusion criteria
Patient is 18 years or older
Patient is willing and able to provide written informed consent
Patient is willing and able to complete all scheduled study visits
Diagnosis of migraine, based on the following primary headache characteristics:
At least 5 attacks fulfilling criteria b-d:
Headache attacks lasting 4-72 hours (untreated or unsuccessfully treated)
Headache has at least two of the following characteristics:
During headache at least one of the following:
Not attributed to another disorder
Exclusion criteria
Primary purpose
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Interventional model
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60 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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