Frovatriptan 2.5mg plus dexketoprofen (25mg or 37.5 mg) in menstrually related migraine. Subanalysis from a double-blind, randomized trial

G. Allais; G. Bussone; V. Tullo; P. Cortelli; F. Valguarnera; P. Barbanti; G. Sette; F. D'Onofrio; M. Curone; C. Benedetto

doi:10.1177/0333102414542290

Frovatriptan 2.5mg plus dexketoprofen (25mg or 37.5 mg) in menstrually related migraine. Subanalysis from a double-blind, randomized trial

G. Allais, G. Bussone, V. Tullo, P. Cortelli, F. Valguarnera, P. Barbanti, G. Sette, F. D'Onofrio, M. Curone, C. Benedetto

Research output: Contribution to journal › Article › peer-review

Abstract

Purpose: The purpose of this article is to investigate the efficacy and safety of frovatriptan plus dexketoprofen 25 or 37.5 mg (FroDex25 or FroDex37.5, respectively) compared to that of frovatriptan 2.5 mg (Frova) in menstrually related migraine (MRM). Aim: The aim of this article is to analyze a subgroup of 76 women who treated an MRM attack in this multicenter, randomized, double-blind, parallel-group study. Methods: The primary end-point was the proportion of patients who were pain free (PF) at two hours. Secondary endpoints included pain-relief (PR) at two hours and 48 hours sustained pain free (SPF). Results: PF rates at two hours were 29% under Frova, 48% under FroDex25 and 64% under FroDex37.5 (p

Original language	English
Pages (from-to)	45-50
Number of pages	6
Journal	Cephalalgia
Volume	35
Issue number	1
DOIs	https://doi.org/10.1177/0333102414542290
Publication status	Published - 2015

Keywords

Dexketoprofen
Frovatriptan
Menstrually related migraine
Migraine attacks

ASJC Scopus subject areas

Clinical Neurology

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10.1177/0333102414542290

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Frovatriptan 2.5mg plus dexketoprofen (25mg or 37.5 mg) in menstrually related migraine. Subanalysis from a double-blind, randomized trial. / Allais, G.; Bussone, G.; Tullo, V.; Cortelli, P.; Valguarnera, F.; Barbanti, P.; Sette, G.; D'Onofrio, F.; Curone, M.; Benedetto, C.

In: Cephalalgia, Vol. 35, No. 1, 2015, p. 45-50.

Research output: Contribution to journal › Article › peer-review

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abstract = "Purpose: The purpose of this article is to investigate the efficacy and safety of frovatriptan plus dexketoprofen 25 or 37.5 mg (FroDex25 or FroDex37.5, respectively) compared to that of frovatriptan 2.5 mg (Frova) in menstrually related migraine (MRM). Aim: The aim of this article is to analyze a subgroup of 76 women who treated an MRM attack in this multicenter, randomized, double-blind, parallel-group study. Methods: The primary end-point was the proportion of patients who were pain free (PF) at two hours. Secondary endpoints included pain-relief (PR) at two hours and 48 hours sustained pain free (SPF). Results: PF rates at two hours were 29% under Frova, 48% under FroDex25 and 64% under FroDex37.5 (p",

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AU - Allais, G.

AU - Bussone, G.

AU - Tullo, V.

AU - Cortelli, P.

AU - Valguarnera, F.

AU - Barbanti, P.

AU - Sette, G.

AU - D'Onofrio, F.

AU - Curone, M.

AU - Benedetto, C.

PY - 2015

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N2 - Purpose: The purpose of this article is to investigate the efficacy and safety of frovatriptan plus dexketoprofen 25 or 37.5 mg (FroDex25 or FroDex37.5, respectively) compared to that of frovatriptan 2.5 mg (Frova) in menstrually related migraine (MRM). Aim: The aim of this article is to analyze a subgroup of 76 women who treated an MRM attack in this multicenter, randomized, double-blind, parallel-group study. Methods: The primary end-point was the proportion of patients who were pain free (PF) at two hours. Secondary endpoints included pain-relief (PR) at two hours and 48 hours sustained pain free (SPF). Results: PF rates at two hours were 29% under Frova, 48% under FroDex25 and 64% under FroDex37.5 (p

AB - Purpose: The purpose of this article is to investigate the efficacy and safety of frovatriptan plus dexketoprofen 25 or 37.5 mg (FroDex25 or FroDex37.5, respectively) compared to that of frovatriptan 2.5 mg (Frova) in menstrually related migraine (MRM). Aim: The aim of this article is to analyze a subgroup of 76 women who treated an MRM attack in this multicenter, randomized, double-blind, parallel-group study. Methods: The primary end-point was the proportion of patients who were pain free (PF) at two hours. Secondary endpoints included pain-relief (PR) at two hours and 48 hours sustained pain free (SPF). Results: PF rates at two hours were 29% under Frova, 48% under FroDex25 and 64% under FroDex37.5 (p

KW - Dexketoprofen

KW - Frovatriptan

KW - Menstrually related migraine

KW - Migraine attacks

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Frovatriptan 2.5mg plus dexketoprofen (25mg or 37.5 mg) in menstrually related migraine. Subanalysis from a double-blind, randomized trial

Abstract

Keywords

ASJC Scopus subject areas

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