Randomised trial on episodic cluster headache with an angiotensin II receptor blocker

Erling Tronvik, Troels Wienecke, Inge Monstad, Carl Dahløf, Magne Geir Bøe, Anne Bolette Tjensvoll, Rolf Salvesen, John Anker Zwart, Sven Olof Jansson, Lars Jacob Stovner

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Abstrakt

Objectives: The aim of this study was to evaluate the angiotensin II receptor antagonist candesartan as prophylactic medication in patients with episodic cluster headache. Methods: This study comprised a prospective, placebo-controlled, double-blind, parallel-designed trial performed in seven centres in Scandinavia. Forty (40) patients with episodic cluster headache (ICHD-2) were recruited and randomised over a five-year period to placebo or 16 mg candesartan in the first week, and placebo or 32 mg candesartan in the second and third week. Results: The number of cluster headache attacks (primary efficacy variable) during the three-week treatment period was reduced from 14.3±9.2 attacks in week 1 to 5.6±7.0 attacks in week 3 (±61%) in the candesartan group and from 16.8±14.1 attacks in week 1 to 10.5±11.3 attacks in week 3 (±38%) in the placebo group. The difference between the candesartan and placebo group was not significant with the pre-planned non-parametric ranking test, but a post-hoc exact Poisson test, which takes into account the temporal properties of the data, revealed a significant result (p<0.0001). Conclusions: This was a negative trial. Post-hoc statistics suitable to describe the temporal changes in cluster headache indicate that conduction of future larger studies may be justified.

OriginalsprogEngelsk
Sider (fra-til)1026-1034
Antal sider9
TidsskriftCephalalgia
Vol/bind33
Udgave nummer12
DOI
StatusUdgivet - sep. 2013

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Udforsk hvilke forskningsemner 'Randomised trial on episodic cluster headache with an angiotensin II receptor blocker' indeholder.

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