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Harald Schrader Norwegian University of Science and
Technology, Department of Neurology, 7006 Trondheim, Norway
Correspondence to:
H Schrader harald.schrader{at}medisin.ntnu.no
Objective:
To determine the efficacy of an angiotensin converting enzyme inhibitor in the prophylaxis of migraine.
Design:
Double blind, placebo controlled, crossover study.
Setting:
Neurological outpatient clinic.
Participants:
Sixty patients aged 19-59 years with
migraine with two to six episodes a month.
Interventions:
Treatment period of 12 weeks with one
10 mg lisinopril tablet once daily for one week then two 10 mg
lisinopril tablets once daily for 11 weeks, followed by a two week wash
out period. Second treatment period of one placebo tablet once daily for one week and then two placebo tablets for 11 weeks. Thirty participants followed this schedule, and 30 received placebo followed by lisinopril.
Main outcome measures:
Primary end points: number of
hours with headache, number of days with headache, number of days with
migraine. Secondary end points: headache severity index, use of drugs
for symptomatic relief, quality of life and number of days taken as
sick leave, acceptability of treatment.
Results:
In the 47 participants with complete data, hours with headache, days with headache, days with migraine, and headache severity index were significantly reduced by 20% (95% confidence interval 5% to 36%), 17% (5% to 30%), 21% (9% to
34%), and 20% (3% to 37%), respectively, with lisinopril compared
with placebo. Days with migraine were reduced by at least 50% in 14 participants for active treatment versus placebo and 17 patients for
active treatment versus run-in period. Days with migraine were fewer by
at least 50% in 14 participants for active treatment versus placebo.
Intention to treat analysis of data from 55 patients supported the
differences in favour of lisinopril for the primary end points.
Conclusion:
The angiotensin converting enzyme
inhibitor, lisinopril, has a clinically important prophylactic effect
in migraine.
© BMJ 2001
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