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Evaluation of a New Treatment for Migraine Attacks

K

Karolinska University Hospital

Status

Completed

Conditions

Migraine

Treatments

Device: Migraine Medical Device
Device: Inactive Migraine Medical Device

Study type

Interventional

Funder types

Other

Identifiers

NCT01880671
Migraine2013/657-32

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy of a novel therapy for treatment of migraine, pain reduction and relief of associated symptoms during ongoing migraine attacks, and presence of a preventive effect post treatment.

Enrollment

36 patients

Sex

All

Ages

20 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female or male subjects, in otherwise good health, 20 to 55 years of age
  • Subjects who meet the ICHD-2 (2nd Edition of The International Headache Classification) criteria for migraine headache
  • Subjects with a minimum of 1 migraine attack per month
  • Attack duration of 4 to 72 hours
  • Normal attack intensity of at least 4 on a 0-10 VAS-scale

Exclusion criteria

  • Completed heart surgery
  • Cardiovascular disease
  • Vascular damage on neck vessels
  • Disease other than migraine of the CSN
  • Severe disease of vital body organs
  • Severe psychiatric disorders
  • More than 6 migraine attacks per month

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

36 participants in 2 patient groups, including a placebo group

Migraine Medical Device
Experimental group
Treatment:
Device: Migraine Medical Device
Inactive Migraine Medical Device
Placebo Comparator group
Treatment:
Device: Inactive Migraine Medical Device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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