TY - JOUR
T1 - Timolol vs propranolol vs placebo in common migraine prophylaxis
T2 - a double‐blind multicenter trial
AU - Tfelt‐Hansen, P.
AU - Standnes, B.
AU - Kangasneimi, P.
AU - Hakkarainen, H.
AU - Olesen, J.
PY - 1984/1
Y1 - 1984/1
N2 - ABSTRACT— Common migraine sufferers (25 males, 71 females) with a history of 2–6 attacks per month participated in a 4‐centre trial comparing the prophylactic effect of timolol (10 mg b.i.d.) and propranolol (80 mg b.i.d.) to placebo. After a pretreatment period of 4 weeks they entered a double‐blind 3‐way cross‐over trial with 3 treatment periods of 12 weeks each. 83 patients received all 3 treatments. The mean frequency of attacks per 28 days was 3.35** on timolol, 3.69** on propranolol and 4.83 on placebo. Mean severity of attacks (0–3) was 1.75 on timolol*, 1.83 on propranolol, and 1.93 on placebo. Mean duration of attacks was 7.41 h on timolol, 7.38 on propranolol and 7.95 on placebo. The headache index (frequency times severity) was 5.71** on timolol, 6.66** on propranolol and 9.03 on placebo (*P < 0.05, **P < 0.01 compared to placebo). The difference between propranolol and timolol was non‐significant: frequency of attacks 0.34 (95% confidence limits ‐ 0.26; 0.89). Headache index 0.95 (95% confidence limits ‐ 0.43; 1.97). 38 patients on timolol, 35 patients on propranolol and 23 patients on placebo experienced side effects (P < 0.05). It is concluded that timolol and propranolol are equally effective in the used doses (1:8) for common migraine prophylaxis.
AB - ABSTRACT— Common migraine sufferers (25 males, 71 females) with a history of 2–6 attacks per month participated in a 4‐centre trial comparing the prophylactic effect of timolol (10 mg b.i.d.) and propranolol (80 mg b.i.d.) to placebo. After a pretreatment period of 4 weeks they entered a double‐blind 3‐way cross‐over trial with 3 treatment periods of 12 weeks each. 83 patients received all 3 treatments. The mean frequency of attacks per 28 days was 3.35** on timolol, 3.69** on propranolol and 4.83 on placebo. Mean severity of attacks (0–3) was 1.75 on timolol*, 1.83 on propranolol, and 1.93 on placebo. Mean duration of attacks was 7.41 h on timolol, 7.38 on propranolol and 7.95 on placebo. The headache index (frequency times severity) was 5.71** on timolol, 6.66** on propranolol and 9.03 on placebo (*P < 0.05, **P < 0.01 compared to placebo). The difference between propranolol and timolol was non‐significant: frequency of attacks 0.34 (95% confidence limits ‐ 0.26; 0.89). Headache index 0.95 (95% confidence limits ‐ 0.43; 1.97). 38 patients on timolol, 35 patients on propranolol and 23 patients on placebo experienced side effects (P < 0.05). It is concluded that timolol and propranolol are equally effective in the used doses (1:8) for common migraine prophylaxis.
KW - Adrenergic beta‐receptor‐blockaders
KW - clinical trials
KW - migraine
KW - propranolol
KW - timolol
UR - http://www.scopus.com/inward/record.url?scp=0021357487&partnerID=8YFLogxK
U2 - 10.1111/j.1600-0404.1984.tb07772.x
DO - 10.1111/j.1600-0404.1984.tb07772.x
M3 - Journal article
C2 - 6367336
AN - SCOPUS:0021357487
SN - 0001-6314
VL - 69
SP - 1
EP - 8
JO - Acta Neurologica Scandinavica
JF - Acta Neurologica Scandinavica
IS - 1
ER -