TY - JOUR
T1 - Memantine for Prophylactic Treatment of Migraine Without Aura
T2 - A Randomized Double-Blind Placebo-Controlled Study
AU - Noruzzadeh, Rezvan
AU - Modabbernia, Amirhossein
AU - Aghamollaii, Vajiheh
AU - Ghaffarpour, Majid
AU - Harirchian, Mohammad Hossein
AU - Salahi, Sarvenaz
AU - Nikbakht, Nikta
AU - Noruzi, Nahid
AU - Tafakhori, Abbas
N1 - Publisher Copyright:
© 2015 American Headache Society.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Background Uncontrolled studies in human have suggested that memantine might be a suitable option for migraine prophylaxis. Objective To assess the efficacy and tolerability of memantine for migraine prophylaxis. Methods This was a 12-week randomized double-blind placebo-controlled parallel-group study. Sixty patients with migraine without aura were randomized using a computer-generated list to receive memantine (10 mg/day) or placebo for 12 weeks. The primary outcome was the difference in change from baseline in the monthly attack frequency at week 12 between the two groups (using migraine diary). Secondary efficacy measures were assessed using several clinical, functional, and psychological instruments. We performed both complete case (CC) and intention-to-treat analyses (ITT). Results Twenty-five patients in the memantine group and 27 patients in the placebo group completed the study. Patients in the memantine group showed significantly greater reduction (mean change; 3.4; 95%CI, 2.3-4.4) in the monthly attack frequency than the placebo group (mean change, 1.0; 95%CI, 0.3-1.7) (mean difference [MD], 2.3; 95%CI, 1.1-3.5, P <.001). Both CC (MD, 4.9; 95%CI, 2.6-7.2 days), and ITT analyses (MD, 5.2; 95%CI, 2.0-8.5) showed significantly higher reduction in the mean number of migraine days in the memantine group than the placebo group (P <.01). Patients in the memantine group experienced greater reduction in the number of work absence days, severity, and disability score than the patients in the placebo group in both ITT and CC analyses. Changes in quality of life, sleep, depression, and anxiety did not differ between the two groups. Three patients in the memantine group complained of sedation, mild vertigo and nausea, and drowsiness. In the placebo group, one patient complained of nausea and another patient discontinued treatment after 2 weeks due to vertigo. Conclusion Memantine might be a tolerable and efficacious option for prophylaxis in patients with migraine without aura. Tolerability, short duration required for titration, and safety profile in pregnancy might give memantine an advantage over other antimigraine medications. The study was registered in the Iranian Registry of Clinical Trials (Registration number: IRCT2013120115616N1).
AB - Background Uncontrolled studies in human have suggested that memantine might be a suitable option for migraine prophylaxis. Objective To assess the efficacy and tolerability of memantine for migraine prophylaxis. Methods This was a 12-week randomized double-blind placebo-controlled parallel-group study. Sixty patients with migraine without aura were randomized using a computer-generated list to receive memantine (10 mg/day) or placebo for 12 weeks. The primary outcome was the difference in change from baseline in the monthly attack frequency at week 12 between the two groups (using migraine diary). Secondary efficacy measures were assessed using several clinical, functional, and psychological instruments. We performed both complete case (CC) and intention-to-treat analyses (ITT). Results Twenty-five patients in the memantine group and 27 patients in the placebo group completed the study. Patients in the memantine group showed significantly greater reduction (mean change; 3.4; 95%CI, 2.3-4.4) in the monthly attack frequency than the placebo group (mean change, 1.0; 95%CI, 0.3-1.7) (mean difference [MD], 2.3; 95%CI, 1.1-3.5, P <.001). Both CC (MD, 4.9; 95%CI, 2.6-7.2 days), and ITT analyses (MD, 5.2; 95%CI, 2.0-8.5) showed significantly higher reduction in the mean number of migraine days in the memantine group than the placebo group (P <.01). Patients in the memantine group experienced greater reduction in the number of work absence days, severity, and disability score than the patients in the placebo group in both ITT and CC analyses. Changes in quality of life, sleep, depression, and anxiety did not differ between the two groups. Three patients in the memantine group complained of sedation, mild vertigo and nausea, and drowsiness. In the placebo group, one patient complained of nausea and another patient discontinued treatment after 2 weeks due to vertigo. Conclusion Memantine might be a tolerable and efficacious option for prophylaxis in patients with migraine without aura. Tolerability, short duration required for titration, and safety profile in pregnancy might give memantine an advantage over other antimigraine medications. The study was registered in the Iranian Registry of Clinical Trials (Registration number: IRCT2013120115616N1).
KW - glutamate
KW - memantine
KW - migraine without aura
KW - placebo
KW - prophylaxis
KW - randomized controlled trial
UR - http://www.scopus.com/inward/record.url?scp=84956763293&partnerID=8YFLogxK
U2 - 10.1111/head.12732
DO - 10.1111/head.12732
M3 - Article
C2 - 26638119
AN - SCOPUS:84956763293
SN - 0017-8748
VL - 56
SP - 95
EP - 103
JO - Headache
JF - Headache
IS - 1
ER -