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Symptoms of cutaneous sensitivity pre-treatment and post-treatment: results from the rizatriptan TAME studies.

Abstract
The presence of cutaneous allodynia may predict response to triptans. Identical randomized double-blind studies were conducted comparing the efficacy of rizatriptan 10 mg or placebo administered within 1 h of headache onset, while pain was mild. The primary endpoint was freedom from pain at 2 h. Presence of symptoms suggesting cutaneous sensitivity (SCS) at baseline and at 2 h post-treatment was recorded. Before treatment, 29% of rizatriptan patients and 22% of placebo patients reported SCS. At 2 h, the percentage of patients with SCS was significantly decreased with rizatriptan. The presence of SCS pre-treatment was not predictive of response to rizatriptan. Most patients with SCS at 2 h were non-responders. Early treatment with rizatriptan significantly reduced the percentage of patients with SCS at 2 h. The presence of SCS at baseline did not predict pain-free response, but presence of SCS at 2 h correlated with lack of a 2-h pain-free response.
AuthorsR Cady, V Martin, A Mauskop, A Rodgers, C M Hustad, K E Ramsey, F Skobieranda
JournalCephalalgia : an international journal of headache (Cephalalgia) Vol. 27 Issue 9 Pg. 1055-60 (Sep 2007) ISSN: 0333-1024 [Print] England
PMID17681023 (Publication Type: Journal Article, Randomized Controlled Trial)
Chemical References
  • Serotonin Receptor Agonists
  • Triazoles
  • Tryptamines
  • rizatriptan
Topics
  • Adult
  • Comorbidity
  • Double-Blind Method
  • Female
  • Headache (drug therapy, epidemiology)
  • Humans
  • Hyperalgesia (drug therapy, epidemiology)
  • Male
  • Migraine Disorders (drug therapy, epidemiology)
  • Placebo Effect
  • Prevalence
  • Randomized Controlled Trials as Topic
  • Risk Assessment (methods)
  • Risk Factors
  • Serotonin Receptor Agonists (therapeutic use)
  • Touch
  • Treatment Outcome
  • Triazoles (therapeutic use)
  • Tryptamines (therapeutic use)
  • United States (epidemiology)

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