TY - JOUR
T1 - Frovatriptan versus other triptans in the acute treatment of migraine
T2 - Pooled analysis of three double-blind, randomized, cross-over, multicenter, Italian studies
AU - Cortelli, Pietro
AU - Allais, Gianni
AU - Tullo, Vincenzo
AU - Benedetto, Chiara
AU - Zava, Dario
AU - Omboni, Stefano
AU - Bussone, Gennaro
PY - 2011/5
Y1 - 2011/5
N2 - The objective of the study is to systematically review the efficacy and safety of frovatriptan (F) versus rizatriptan (R), zolmitriptan (Z) and almotriptan (A), through a pooled analysis of three individual studies. 414 subjects with a history of migraine with or without aura (IHS criteria) were randomized to F 2.5 mg or R 10 mg (study 1), F 2.5 mg or Z 2.5 mg (study 2), and F 2.5 mg or A 12.5 mg (study 3). The studies had an identical multicenter, randomized, double blind, cross-over design, with each of the two treatment periods lasting not more than 3 months. The number of pain free (PF) and pain relief (PR) episodes at 2 h, and the number of sustained pain free (SPF) and recurrent episodes within the 48 h were the efficacy endpoints. 346 patients were included in the intention-totreat analysis. Rate of PF episodes at 2 h was 30% with F and 34% with comparators (p = NS). PR episodes at 2 h were 55% for F and 59% for comparators (p = NS). SPF episodes at 48 h were also similar between the two groups (22% F vs. 21% comparators). Rate of recurrence was significantly (p
AB - The objective of the study is to systematically review the efficacy and safety of frovatriptan (F) versus rizatriptan (R), zolmitriptan (Z) and almotriptan (A), through a pooled analysis of three individual studies. 414 subjects with a history of migraine with or without aura (IHS criteria) were randomized to F 2.5 mg or R 10 mg (study 1), F 2.5 mg or Z 2.5 mg (study 2), and F 2.5 mg or A 12.5 mg (study 3). The studies had an identical multicenter, randomized, double blind, cross-over design, with each of the two treatment periods lasting not more than 3 months. The number of pain free (PF) and pain relief (PR) episodes at 2 h, and the number of sustained pain free (SPF) and recurrent episodes within the 48 h were the efficacy endpoints. 346 patients were included in the intention-totreat analysis. Rate of PF episodes at 2 h was 30% with F and 34% with comparators (p = NS). PR episodes at 2 h were 55% for F and 59% for comparators (p = NS). SPF episodes at 48 h were also similar between the two groups (22% F vs. 21% comparators). Rate of recurrence was significantly (p
KW - Almotriptan
KW - Frovatriptan
KW - Migraine
KW - Rizatriptan
KW - Zolmitriptan
UR - http://www.scopus.com/inward/record.url?scp=79960145588&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79960145588&partnerID=8YFLogxK
U2 - 10.1007/s10072-011-0551-2
DO - 10.1007/s10072-011-0551-2
M3 - Article
C2 - 21533722
AN - SCOPUS:79960145588
SN - 1590-1874
VL - 32
JO - Neurological Sciences
JF - Neurological Sciences
IS - SUPPL. 1
ER -