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Optical Treatment of Migraines Using the Avulux™ Optical Filter in the Form of Spectacle Lenses.

A

Avulux

Status

Completed

Conditions

Migraine

Treatments

Device: Sham Spectacles
Other: HIT-6 Questionnaire
Device: Avulux Spectacles

Study type

Interventional

Funder types

Industry

Identifiers

NCT03902496
20190592

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient is 18 years or older

  2. Patient is willing and able to provide written informed consent

  3. Patient is willing and able to complete all scheduled study visits

  4. Diagnosis of migraine, based on the following primary headache characteristics:

    1. At least 5 attacks fulfilling criteria b-d:

    2. Headache attacks lasting 4-72 hours (untreated or unsuccessfully treated)

    3. Headache has at least two of the following characteristics:

      • unilateral location
      • pulsating quality
      • moderate or severe pain intensity
      • aggravation by or causing avoidance of routine physical activity (eg, walking or climbing stairs)
    4. During headache at least one of the following:

      • nausea and/or vomiting
      • photophobia and phonophobia
    5. Not attributed to another disorder

Exclusion criteria

  1. Patients with other light sensitive conditions, such as iritis.
  2. Patients who have less than 4 headache days per month
  3. Patients who have chronic daily headaches.
  4. Patients who have had any change in their migraine treatment within the 4 weeks prior to the trial onset.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Avulux Spectacles
Experimental group
Description:
Subjects will be instructed to use the spectacles for three weeks. They will be instructed to put the spectacles on at the first signs or symptoms of their migraine attacks. This could be their usual aura, or the first signs of their headache commencing, and to keep the spectacles on until their headache has resolved.
Treatment:
Device: Avulux Spectacles
Other: HIT-6 Questionnaire
Sham Spectacles
Sham Comparator group
Description:
Subjects will be instructed to use the spectacles for three weeks. They will be instructed to put the spectacles on at the first signs or symptoms of their migraine attacks. This could be their usual aura, or the first signs of their headache commencing, and to keep the spectacles on until their headache has resolved.
Treatment:
Other: HIT-6 Questionnaire
Device: Sham Spectacles

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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