Cyproheptadine hydrochloride (CH) is rarely used to treat adult patients with
migraine in Japan because it causes
sleepiness. In this study, we investigated the preventive effect of CH in 12 patients who had failed to respond to conventional preventive treatments among 103
migraine patients treated at our hospital. These 12 subjects had all received unsuccessful
migraine prophylaxis with
lomerizine,
valproic acid and
topiramate, or had discontinued these treatments due to adverse reactions. Initially, the subjects were given 4 mg CH before sleeping. In those who experienced no clinically significant
sleepiness following the treatment, the
drug was orally administered at 4 mg after breakfast as well (8 mg per day in total).
Drug efficacy was evaluated by examining the frequency of
migraine at one month and three months after the start of treatment. The frequency of
migraine was dramatically reduced in all patients within 7 to 10 days after starting treatment. The average frequency of
migraine during the three-month period was 2.6 episodes per month, representing a significant (p < 0.01) reduction from the pretreatment frequency of over 10 per month. Our results indicate that CH may be effective as a
migraine-preventive treatment for patients in whom conventional drugs have been ineffective or have caused side effects. But this study is not a double blind randomized trial, and an open study with no control group.