Frovatriptan as preemptive treatment for fasting-induced migraine

Headache. 2011 Mar;51(3):369-374. doi: 10.1111/j.1526-4610.2010.01827.x. Epub 2011 Jan 26.

Abstract

Objective: To examine frovatriptan's efficacy as preemptive treatment for fasting-induced migraine.

Background: Fasting is a common migraine trigger that cannot always be avoided. The development of a short-term preemptive approach would be of benefit. Because of its longer half-life, frovatriptan has been effectively used for short-term daily use to prevent menstrually related migraines and might prove useful in the prevention of fasting-induced migraine.

Methods: This was a double-blind, placebo-controlled, randomized, parallel-group trial.

Subjects: With a history of fasting-induced episodic migraine were randomly assigned to receive either frovatriptan (5.0 mg) or placebo (ratio 1:1).

Subjects: Took a single dose of study medication at the start of their 20-hour fast. Information about headache intensity, associated symptoms, and use of rescue medication was captured at defined time points from the start of the fast through 20 hours post-fast.

Results: Of the 75 subjects screened, 74 subjects were randomized and 71 subjects completed the study. Demographic characteristics of the placebo and frovatriptan treatment groups were not statistically different. Thirty-three subjects received active drug. Twelve (36.4%) developed a headache between 6 and 20 hours after the start of the fast (1/33 mild, 11/33 moderate or severe). In the placebo group, 18/34 (52.9%) developed a headache (4/34 mild, 14/34 moderate or severe). The difference between the 2 treatment groups did not achieve statistical significance; Pearson chi-square, P = .172. Kaplan-Meier survival analysis showed no difference between the 2 treatment groups with respect to the time of onset of headache of any intensity (log rank, P = .264) and for the time of onset of a moderate or severe intensity (log rank, P = .634).

Conclusion: More subjects on placebo developed a headache than those on frovatriptan. Perhaps because of the small number of subjects involved, the differences in headache incidences observed did not achieve statistical significance.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carbazoles / administration & dosage
  • Carbazoles / adverse effects
  • Carbazoles / therapeutic use*
  • Double-Blind Method
  • Drug Administration Schedule
  • Fasting / adverse effects*
  • Female
  • Half-Life
  • Humans
  • Incidence
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Migraine Disorders / epidemiology
  • Migraine Disorders / etiology*
  • Migraine Disorders / prevention & control*
  • Pilot Projects
  • Serotonin Receptor Agonists / adverse effects
  • Serotonin Receptor Agonists / therapeutic use*
  • Time Factors
  • Treatment Outcome
  • Tryptamines / administration & dosage
  • Tryptamines / adverse effects
  • Tryptamines / therapeutic use*

Substances

  • Carbazoles
  • Serotonin Receptor Agonists
  • Tryptamines
  • frovatriptan