Timolol vs propranolol vs placebo in common migraine prophylaxis: a double-blind multicenter trial.

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 less than 0.05, P less than 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 propranolol and 23 patients on placebo experienced side effects (P less than 0.05). It is concluded that timolol and propranolol are equally effective in the used doses (1:8) for common migraine prophylaxis.

• Authors: P Tfelt-Hansen, B Standnes, P Kangasneimi, H Hakkarainen, J Olesen
• Journal: Acta neurologica Scandinavica (Acta Neurol Scand) Vol. 69 Issue 1 Pg. 1-8 (Jan 1984) ISSN: 0001-6314 [Print] Denmark
• PMID: 6367336 (Publication Type: Clinical Trial, Comparative Study, Journal Article)

Chemical References

• Timolol
• Propranolol

Topics

• Adolescent
• Adult
• Aged
• Clinical Trials as Topic
• Double-Blind Method
• Female
• Humans
• Male
• Middle Aged
• Migraine Disorders (prevention & control)
• Propranolol (adverse effects, therapeutic use)
• Random Allocation
• Timolol (adverse effects, therapeutic use)