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Can topical timolol maleate ophthalmic solution reduce pain scores after an acute migraine attack better than placebo eyedrops?
In a randomized crossover clinical trial involving 50 patients, topical timolol was more likely to reduce pain scores 20 minutes after instillation compared with placebo.
These findings support consideration of timolol eyedrops in the management of acute migraine attacks, but confirmation for longer follow-up with larger groups at multiple sites is warranted.
Oral β-blockers used for the prevention of migraine headache are not effective for the treatment of acute pain. Small case series have suggested that topically applied β-blockers may be useful in the management of acute migraine pain, warranting evaluation with randomized clinical trials.
To evaluate the short-term efficacy and safety of topically applied timolol maleate ophthalmic solution, 0.5%, compared with topically applied placebo eyedrops in the treatment of acute migraine attacks.
Design, Setting, and Participants
In this randomized, masked placebo-controlled crossover trial conducted from May 27, 2015, to August 28, 2017, 50 patients with migraine were randomized to receive either timolol eyedrops, 0.5%, or a placebo eyedrop (carboxymethyl cellulose, 0.5%). After a 3-month treatment period, patients completed a 1-month washout period and were crossed over to receive the opposite treatment for a final 3 months. Analysis was performed on a modified intent-to-treat basis.
After random assignment, patients were instructed to use 1 drop of the assigned medication in each eye at the earliest onset of migraine.
Main Outcomes and Measures
The main outcome measure was reduction in pain score with treatment. The primary end point was reduction of pain score by 4 points, or to zero, 20 minutes after instillation of the eyedrop.
Of the 50 patients, 42 (84%) were females and the mean (SD) age was 27.3 (11.3) years. Of a total of 619 migraine attacks, 284 (46%) were treated with timolol, 271 (44%) were treated with the placebo, and 64 (10%) occurred during the washout period when no study medications were used. Seven patients (14%) withdrew after randomization. A total of 233 of the timolol-treated migraine attacks (82%) were associated with a reduction in pain score by 4 points, or to zero, at 20 minutes compared with 38 of the placebo-treated attacks (14%), with a difference of 68 percentage points (95% CI, 62-74 percentage points). A generalized estimating equation analysis revealed that pain score reduction at 20 minutes was greater in the timolol group compared with the placebo group by a mean (SE) of 4.63 points (0.34) (P < .001).
Conclusions and Relevance
This randomized crossover trial supports consideration of timolol eyedrops in the acute treatment of migraine. Further research is warranted to determine if the improvements observed are sustained for a longer follow-up and with larger groups.
CTRI/2015/05/005829, UTN: U1111-1167-6439
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CME Disclosure Statement: Unless noted, all individuals in control of content reported no relevant financial relationships. If applicable, all relevant financial relationships have been mitigated.
Accepted for Publication: August 10, 2020.
Corresponding Author: Abraham Kurian, MS, DO, Chaithanya Eye Hospital and Research Institute, Kesavadasapuram, Trivandrum, Kerala 695004, India (email@example.com).
Published Online: October 1, 2020. doi:10.1001/jamaophthalmol.2020.3676
Author Contributions: Drs Kurian and Reghunadhan had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Kurian, Reghunadhan, Nair.
Acquisition, analysis, or interpretation of data: Kurian, Reghunadhan, Thilak, Soman.
Drafting of the manuscript: Kurian, Reghunadhan, Thilak.
Critical revision of the manuscript for important intellectual content: Kurian, Reghunadhan, Soman, Nair.
Statistical analysis: Reghunadhan, Soman.
Administrative, technical, or material support: Kurian, Thilak.
Supervision: Kurian, Nair.
Conflict of Interest Disclosures: None reported.
Data Sharing Statement: See Supplement 3.
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